EP3681949A1 - Fluorinated copolymer and compositions and articles including the same - Google Patents
Fluorinated copolymer and compositions and articles including the sameInfo
- Publication number
- EP3681949A1 EP3681949A1 EP18857361.2A EP18857361A EP3681949A1 EP 3681949 A1 EP3681949 A1 EP 3681949A1 EP 18857361 A EP18857361 A EP 18857361A EP 3681949 A1 EP3681949 A1 EP 3681949A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- copolymer
- formula
- present disclosure
- divalent units
- represented
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Withdrawn
Links
- 229920001577 copolymer Polymers 0.000 title claims abstract description 276
- 239000000203 mixture Substances 0.000 title description 20
- 239000012528 membrane Substances 0.000 claims abstract description 61
- 239000003054 catalyst Substances 0.000 claims abstract description 45
- 239000001257 hydrogen Substances 0.000 claims abstract description 30
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 30
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims abstract description 30
- 239000005518 polymer electrolyte Substances 0.000 claims abstract description 30
- 229910052799 carbon Inorganic materials 0.000 claims abstract description 24
- 229910006095 SO2F Inorganic materials 0.000 claims abstract description 17
- 239000000155 melt Substances 0.000 claims abstract description 13
- 230000007704 transition Effects 0.000 claims abstract description 12
- -1 alkali-metal cation Chemical class 0.000 claims description 82
- 125000004432 carbon atom Chemical group C* 0.000 claims description 46
- 125000000217 alkyl group Chemical group 0.000 claims description 22
- 125000005010 perfluoroalkyl group Chemical group 0.000 claims description 22
- 229910052783 alkali metal Inorganic materials 0.000 claims description 19
- 125000001453 quaternary ammonium group Chemical group 0.000 claims description 15
- HCDGVLDPFQMKDK-UHFFFAOYSA-N hexafluoropropylene Chemical group FC(F)=C(F)C(F)(F)F HCDGVLDPFQMKDK-UHFFFAOYSA-N 0.000 claims description 13
- 230000009477 glass transition Effects 0.000 claims description 8
- UUAGAQFQZIEFAH-UHFFFAOYSA-N chlorotrifluoroethylene Chemical group FC(F)=C(F)Cl UUAGAQFQZIEFAH-UHFFFAOYSA-N 0.000 claims description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 54
- 239000006185 dispersion Substances 0.000 description 46
- 238000000034 method Methods 0.000 description 46
- 229920000642 polymer Polymers 0.000 description 45
- 150000001875 compounds Chemical class 0.000 description 41
- 238000006116 polymerization reaction Methods 0.000 description 41
- MHNPWFZIRJMRKC-UHFFFAOYSA-N 1,1,2-trifluoroethene Chemical compound F[C]=C(F)F MHNPWFZIRJMRKC-UHFFFAOYSA-N 0.000 description 35
- 229910001868 water Inorganic materials 0.000 description 34
- 239000000243 solution Substances 0.000 description 30
- 239000003995 emulsifying agent Substances 0.000 description 29
- 238000006243 chemical reaction Methods 0.000 description 28
- 229920002313 fluoropolymer Polymers 0.000 description 26
- 239000004811 fluoropolymer Substances 0.000 description 26
- 239000000976 ink Substances 0.000 description 26
- 229910052760 oxygen Inorganic materials 0.000 description 26
- 150000003839 salts Chemical class 0.000 description 26
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 25
- 239000001301 oxygen Substances 0.000 description 25
- 239000007787 solid Substances 0.000 description 25
- 229920000554 ionomer Polymers 0.000 description 22
- 239000000178 monomer Substances 0.000 description 21
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 20
- 239000002253 acid Substances 0.000 description 19
- 239000002245 particle Substances 0.000 description 19
- 230000035699 permeability Effects 0.000 description 19
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 15
- QYKIQEUNHZKYBP-UHFFFAOYSA-N Vinyl ether Chemical compound C=COC=C QYKIQEUNHZKYBP-UHFFFAOYSA-N 0.000 description 15
- 239000007789 gas Substances 0.000 description 15
- 150000001768 cations Chemical class 0.000 description 14
- 239000008367 deionised water Substances 0.000 description 14
- 229910021641 deionized water Inorganic materials 0.000 description 14
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 13
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 13
- 229910052684 Cerium Inorganic materials 0.000 description 13
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 13
- 229910000420 cerium oxide Inorganic materials 0.000 description 13
- 239000000446 fuel Substances 0.000 description 13
- 229920000126 latex Polymers 0.000 description 13
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 12
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 12
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 12
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 12
- 239000004816 latex Substances 0.000 description 12
- 229910052751 metal Inorganic materials 0.000 description 12
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 11
- 150000001450 anions Chemical class 0.000 description 11
- GWXLDORMOJMVQZ-UHFFFAOYSA-N cerium Chemical compound [Ce] GWXLDORMOJMVQZ-UHFFFAOYSA-N 0.000 description 11
- 238000000576 coating method Methods 0.000 description 11
- 239000003999 initiator Substances 0.000 description 11
- 239000000463 material Substances 0.000 description 11
- 239000002184 metal Substances 0.000 description 11
- 229910052707 ruthenium Inorganic materials 0.000 description 11
- BQCIDUSAKPWEOX-UHFFFAOYSA-N 1,1-Difluoroethene Chemical compound FC(F)=C BQCIDUSAKPWEOX-UHFFFAOYSA-N 0.000 description 10
- 239000003957 anion exchange resin Substances 0.000 description 10
- 239000003729 cation exchange resin Substances 0.000 description 10
- 239000011248 coating agent Substances 0.000 description 10
- 125000001153 fluoro group Chemical group F* 0.000 description 10
- FAQYAMRNWDIXMY-UHFFFAOYSA-N trichloroborane Chemical compound ClB(Cl)Cl FAQYAMRNWDIXMY-UHFFFAOYSA-N 0.000 description 10
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 9
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 9
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 9
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 9
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 9
- 229910006080 SO2X Inorganic materials 0.000 description 9
- 229910052731 fluorine Inorganic materials 0.000 description 9
- 239000011737 fluorine Substances 0.000 description 9
- 239000011521 glass Substances 0.000 description 9
- 150000002500 ions Chemical class 0.000 description 9
- 229910021645 metal ion Inorganic materials 0.000 description 9
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 9
- 239000002904 solvent Substances 0.000 description 9
- YEJRWHAVMIAJKC-UHFFFAOYSA-N 4-Butyrolactone Chemical compound O=C1CCCO1 YEJRWHAVMIAJKC-UHFFFAOYSA-N 0.000 description 8
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 8
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 8
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 8
- 239000004815 dispersion polymer Substances 0.000 description 8
- 239000003792 electrolyte Substances 0.000 description 8
- 239000000839 emulsion Substances 0.000 description 8
- 238000005342 ion exchange Methods 0.000 description 8
- 238000005259 measurement Methods 0.000 description 8
- 239000003960 organic solvent Substances 0.000 description 8
- BMMGVYCKOGBVEV-UHFFFAOYSA-N oxo(oxoceriooxy)cerium Chemical compound [Ce]=O.O=[Ce]=O BMMGVYCKOGBVEV-UHFFFAOYSA-N 0.000 description 8
- 239000000523 sample Substances 0.000 description 8
- 239000000126 substance Substances 0.000 description 8
- 229910052721 tungsten Inorganic materials 0.000 description 8
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 7
- 125000000129 anionic group Chemical group 0.000 description 7
- 238000005345 coagulation Methods 0.000 description 7
- 230000015271 coagulation Effects 0.000 description 7
- 238000009826 distribution Methods 0.000 description 7
- 238000002296 dynamic light scattering Methods 0.000 description 7
- 150000002170 ethers Chemical class 0.000 description 7
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 description 7
- 238000004519 manufacturing process Methods 0.000 description 7
- 238000007254 oxidation reaction Methods 0.000 description 7
- 238000010998 test method Methods 0.000 description 7
- 238000005406 washing Methods 0.000 description 7
- 229910052727 yttrium Inorganic materials 0.000 description 7
- NWUYHJFMYQTDRP-UHFFFAOYSA-N 1,2-bis(ethenyl)benzene;1-ethenyl-2-ethylbenzene;styrene Chemical compound C=CC1=CC=CC=C1.CCC1=CC=CC=C1C=C.C=CC1=CC=CC=C1C=C NWUYHJFMYQTDRP-UHFFFAOYSA-N 0.000 description 6
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 6
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 6
- WMFOQBRAJBCJND-UHFFFAOYSA-M Lithium hydroxide Chemical compound [Li+].[OH-] WMFOQBRAJBCJND-UHFFFAOYSA-M 0.000 description 6
- 229920001774 Perfluoroether Polymers 0.000 description 6
- 239000011230 binding agent Substances 0.000 description 6
- FJKIXWOMBXYWOQ-UHFFFAOYSA-N ethenoxyethane Chemical compound CCOC=C FJKIXWOMBXYWOQ-UHFFFAOYSA-N 0.000 description 6
- 239000012530 fluid Substances 0.000 description 6
- 238000003682 fluorination reaction Methods 0.000 description 6
- GNOIPBMMFNIUFM-UHFFFAOYSA-N hexamethylphosphoric triamide Chemical compound CN(C)P(=O)(N(C)C)N(C)C GNOIPBMMFNIUFM-UHFFFAOYSA-N 0.000 description 6
- 239000011572 manganese Substances 0.000 description 6
- 239000011159 matrix material Substances 0.000 description 6
- 230000003647 oxidation Effects 0.000 description 6
- 229920001343 polytetrafluoroethylene Polymers 0.000 description 6
- 239000004810 polytetrafluoroethylene Substances 0.000 description 6
- 238000010526 radical polymerization reaction Methods 0.000 description 6
- 239000011347 resin Substances 0.000 description 6
- 229920005989 resin Polymers 0.000 description 6
- 239000011734 sodium Substances 0.000 description 6
- BFKJFAAPBSQJPD-UHFFFAOYSA-N tetrafluoroethene Chemical group FC(F)=C(F)F BFKJFAAPBSQJPD-UHFFFAOYSA-N 0.000 description 6
- 238000012546 transfer Methods 0.000 description 6
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 5
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 5
- ATVJXMYDOSMEPO-UHFFFAOYSA-N 3-prop-2-enoxyprop-1-ene Chemical compound C=CCOCC=C ATVJXMYDOSMEPO-UHFFFAOYSA-N 0.000 description 5
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 5
- KJTLSVCANCCWHF-UHFFFAOYSA-N Ruthenium Chemical compound [Ru] KJTLSVCANCCWHF-UHFFFAOYSA-N 0.000 description 5
- LSNNMFCWUKXFEE-UHFFFAOYSA-N Sulfurous acid Chemical class OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 0.000 description 5
- 238000013019 agitation Methods 0.000 description 5
- 125000003545 alkoxy group Chemical group 0.000 description 5
- 239000007864 aqueous solution Substances 0.000 description 5
- 125000003118 aryl group Chemical group 0.000 description 5
- 125000000732 arylene group Chemical group 0.000 description 5
- 230000015572 biosynthetic process Effects 0.000 description 5
- 229940023913 cation exchange resins Drugs 0.000 description 5
- 125000004122 cyclic group Chemical group 0.000 description 5
- SBZXBUIDTXKZTM-UHFFFAOYSA-N diglyme Chemical compound COCCOCCOC SBZXBUIDTXKZTM-UHFFFAOYSA-N 0.000 description 5
- 230000006870 function Effects 0.000 description 5
- 239000007788 liquid Substances 0.000 description 5
- 229910052748 manganese Inorganic materials 0.000 description 5
- 229910052757 nitrogen Inorganic materials 0.000 description 5
- 239000000047 product Substances 0.000 description 5
- 238000000746 purification Methods 0.000 description 5
- 229910052708 sodium Inorganic materials 0.000 description 5
- 239000000758 substrate Substances 0.000 description 5
- OBTWBSRJZRCYQV-UHFFFAOYSA-N sulfuryl difluoride Chemical compound FS(F)(=O)=O OBTWBSRJZRCYQV-UHFFFAOYSA-N 0.000 description 5
- 229920000049 Carbon (fiber) Polymers 0.000 description 4
- OIFBSDVPJOWBCH-UHFFFAOYSA-N Diethyl carbonate Chemical compound CCOC(=O)OCC OIFBSDVPJOWBCH-UHFFFAOYSA-N 0.000 description 4
- KMTRUDSVKNLOMY-UHFFFAOYSA-N Ethylene carbonate Chemical compound O=C1OCCO1 KMTRUDSVKNLOMY-UHFFFAOYSA-N 0.000 description 4
- 238000005033 Fourier transform infrared spectroscopy Methods 0.000 description 4
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 4
- HBBGRARXTFLTSG-UHFFFAOYSA-N Lithium ion Chemical compound [Li+] HBBGRARXTFLTSG-UHFFFAOYSA-N 0.000 description 4
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 4
- 239000004721 Polyphenylene oxide Substances 0.000 description 4
- 229910006069 SO3H Inorganic materials 0.000 description 4
- FKNQFGJONOIPTF-UHFFFAOYSA-N Sodium cation Chemical compound [Na+] FKNQFGJONOIPTF-UHFFFAOYSA-N 0.000 description 4
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 4
- 150000007513 acids Chemical class 0.000 description 4
- 150000001298 alcohols Chemical class 0.000 description 4
- 125000001931 aliphatic group Chemical group 0.000 description 4
- 150000001340 alkali metals Chemical class 0.000 description 4
- 150000001336 alkenes Chemical class 0.000 description 4
- 238000004458 analytical method Methods 0.000 description 4
- MSMNVXKYCPHLLN-UHFFFAOYSA-N azane;oxalic acid;hydrate Chemical compound N.N.O.OC(=O)C(O)=O MSMNVXKYCPHLLN-UHFFFAOYSA-N 0.000 description 4
- 239000000872 buffer Substances 0.000 description 4
- 239000004917 carbon fiber Substances 0.000 description 4
- 239000000701 coagulant Substances 0.000 description 4
- 238000009792 diffusion process Methods 0.000 description 4
- IEJIGPNLZYLLBP-UHFFFAOYSA-N dimethyl carbonate Chemical compound COC(=O)OC IEJIGPNLZYLLBP-UHFFFAOYSA-N 0.000 description 4
- 229910052736 halogen Inorganic materials 0.000 description 4
- 150000002367 halogens Chemical class 0.000 description 4
- 238000010438 heat treatment Methods 0.000 description 4
- 230000007062 hydrolysis Effects 0.000 description 4
- 238000006460 hydrolysis reaction Methods 0.000 description 4
- 230000003301 hydrolyzing effect Effects 0.000 description 4
- 239000012535 impurity Substances 0.000 description 4
- 150000001457 metallic cations Chemical class 0.000 description 4
- GEVPUGOOGXGPIO-UHFFFAOYSA-N oxalic acid;dihydrate Chemical compound O.O.OC(=O)C(O)=O GEVPUGOOGXGPIO-UHFFFAOYSA-N 0.000 description 4
- 125000004430 oxygen atom Chemical group O* 0.000 description 4
- 125000006551 perfluoro alkylene group Chemical group 0.000 description 4
- 229910052697 platinum Inorganic materials 0.000 description 4
- 229920000570 polyether Polymers 0.000 description 4
- 229920005862 polyol Polymers 0.000 description 4
- 150000003077 polyols Chemical class 0.000 description 4
- 230000008569 process Effects 0.000 description 4
- RUOJZAUFBMNUDX-UHFFFAOYSA-N propylene carbonate Chemical compound CC1COC(=O)O1 RUOJZAUFBMNUDX-UHFFFAOYSA-N 0.000 description 4
- 125000002577 pseudohalo group Chemical group 0.000 description 4
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 4
- 238000011282 treatment Methods 0.000 description 4
- ITMCEJHCFYSIIV-UHFFFAOYSA-N triflic acid Chemical compound OS(=O)(=O)C(F)(F)F ITMCEJHCFYSIIV-UHFFFAOYSA-N 0.000 description 4
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 4
- 229920002554 vinyl polymer Polymers 0.000 description 4
- CYSGHNMQYZDMIA-UHFFFAOYSA-N 1,3-Dimethyl-2-imidazolidinon Chemical compound CN1CCN(C)C1=O CYSGHNMQYZDMIA-UHFFFAOYSA-N 0.000 description 3
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 3
- OJPSFJLSZZTSDF-UHFFFAOYSA-N 3-ethoxyprop-1-ene Chemical compound CCOCC=C OJPSFJLSZZTSDF-UHFFFAOYSA-N 0.000 description 3
- HMBNQNDUEFFFNZ-UHFFFAOYSA-N 4-ethenoxybutan-1-ol Chemical compound OCCCCOC=C HMBNQNDUEFFFNZ-UHFFFAOYSA-N 0.000 description 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 3
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 description 3
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 3
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 3
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
- KRHYYFGTRYWZRS-UHFFFAOYSA-M Fluoride anion Chemical compound [F-] KRHYYFGTRYWZRS-UHFFFAOYSA-M 0.000 description 3
- NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 description 3
- UIHCLUNTQKBZGK-UHFFFAOYSA-N Methyl isobutyl ketone Natural products CCC(C)C(C)=O UIHCLUNTQKBZGK-UHFFFAOYSA-N 0.000 description 3
- FXHOOIRPVKKKFG-UHFFFAOYSA-N N,N-Dimethylacetamide Chemical compound CN(C)C(C)=O FXHOOIRPVKKKFG-UHFFFAOYSA-N 0.000 description 3
- 238000005481 NMR spectroscopy Methods 0.000 description 3
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- 239000011149 active material Substances 0.000 description 3
- 239000003513 alkali Substances 0.000 description 3
- 125000005250 alkyl acrylate group Chemical group 0.000 description 3
- 125000002947 alkylene group Chemical group 0.000 description 3
- 238000005349 anion exchange Methods 0.000 description 3
- 239000002585 base Substances 0.000 description 3
- 229930188620 butyrolactone Natural products 0.000 description 3
- 238000005341 cation exchange Methods 0.000 description 3
- 239000003638 chemical reducing agent Substances 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 238000010276 construction Methods 0.000 description 3
- 239000000356 contaminant Substances 0.000 description 3
- LDHQCZJRKDOVOX-NSCUHMNNSA-N crotonic acid Chemical compound C\C=C\C(O)=O LDHQCZJRKDOVOX-NSCUHMNNSA-N 0.000 description 3
- 230000007423 decrease Effects 0.000 description 3
- 230000003247 decreasing effect Effects 0.000 description 3
- 238000001035 drying Methods 0.000 description 3
- 238000005868 electrolysis reaction Methods 0.000 description 3
- 239000008151 electrolyte solution Substances 0.000 description 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 3
- 238000011156 evaluation Methods 0.000 description 3
- 238000001914 filtration Methods 0.000 description 3
- 229910002804 graphite Inorganic materials 0.000 description 3
- 239000010439 graphite Substances 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 3
- 238000011065 in-situ storage Methods 0.000 description 3
- 229940006487 lithium cation Drugs 0.000 description 3
- 229910001416 lithium ion Inorganic materials 0.000 description 3
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 3
- 229910017604 nitric acid Inorganic materials 0.000 description 3
- 125000002560 nitrile group Chemical group 0.000 description 3
- 230000001590 oxidative effect Effects 0.000 description 3
- 230000000704 physical effect Effects 0.000 description 3
- 229910052700 potassium Inorganic materials 0.000 description 3
- 239000000843 powder Substances 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- CDXZRBLOGJXGTN-UHFFFAOYSA-N prop-2-enoxycyclohexane Chemical compound C=CCOC1CCCCC1 CDXZRBLOGJXGTN-UHFFFAOYSA-N 0.000 description 3
- 238000001228 spectrum Methods 0.000 description 3
- 238000001694 spray drying Methods 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- HXJUTPCZVOIRIF-UHFFFAOYSA-N sulfolane Chemical compound O=S1(=O)CCCC1 HXJUTPCZVOIRIF-UHFFFAOYSA-N 0.000 description 3
- 239000004094 surface-active agent Substances 0.000 description 3
- LDHQCZJRKDOVOX-UHFFFAOYSA-N trans-crotonic acid Natural products CC=CC(O)=O LDHQCZJRKDOVOX-UHFFFAOYSA-N 0.000 description 3
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- WFJINAXLTGKWLB-UHFFFAOYSA-N 1-ethenoxy-1,1,2,2,3,3-hexafluoro-3-(trifluoromethoxy)propane Chemical group FC(F)(F)OC(F)(F)C(F)(F)C(F)(F)OC=C WFJINAXLTGKWLB-UHFFFAOYSA-N 0.000 description 2
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- 150000002642 lithium compounds Chemical class 0.000 description 1
- 229910001540 lithium hexafluoroarsenate(V) Inorganic materials 0.000 description 1
- 229910001496 lithium tetrafluoroborate Inorganic materials 0.000 description 1
- 229910001629 magnesium chloride Inorganic materials 0.000 description 1
- 239000007769 metal material Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- CSSYKHYGURSRAZ-UHFFFAOYSA-N methyl 2,2-difluoroacetate Chemical compound COC(=O)C(F)F CSSYKHYGURSRAZ-UHFFFAOYSA-N 0.000 description 1
- 229910003455 mixed metal oxide Inorganic materials 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 125000000896 monocarboxylic acid group Chemical group 0.000 description 1
- 125000002950 monocyclic group Chemical group 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- 125000001624 naphthyl group Chemical group 0.000 description 1
- 229910021382 natural graphite Inorganic materials 0.000 description 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 1
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 125000002971 oxazolyl group Chemical group 0.000 description 1
- 229910052763 palladium Inorganic materials 0.000 description 1
- 125000006340 pentafluoro ethyl group Chemical group FC(F)(F)C(F)(F)* 0.000 description 1
- 150000002978 peroxides Chemical class 0.000 description 1
- 150000004968 peroxymonosulfuric acids Chemical class 0.000 description 1
- 235000020030 perry Nutrition 0.000 description 1
- JRKICGRDRMAZLK-UHFFFAOYSA-L persulfate group Chemical group S(=O)(=O)([O-])OOS(=O)(=O)[O-] JRKICGRDRMAZLK-UHFFFAOYSA-L 0.000 description 1
- 229920001568 phenolic resin Polymers 0.000 description 1
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 description 1
- 125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 description 1
- 229920003223 poly(pyromellitimide-1,4-diphenyl ether) Polymers 0.000 description 1
- 229920002239 polyacrylonitrile Polymers 0.000 description 1
- 229920005646 polycarboxylate Polymers 0.000 description 1
- 229920002851 polycationic polymer Polymers 0.000 description 1
- 125000003367 polycyclic group Chemical group 0.000 description 1
- 229920001721 polyimide Polymers 0.000 description 1
- 229920005596 polymer binder Polymers 0.000 description 1
- 239000002491 polymer binding agent Substances 0.000 description 1
- 229920002981 polyvinylidene fluoride Polymers 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- 239000011698 potassium fluoride Substances 0.000 description 1
- 235000003270 potassium fluoride Nutrition 0.000 description 1
- BHZRJJOHZFYXTO-UHFFFAOYSA-L potassium sulfite Chemical compound [K+].[K+].[O-]S([O-])=O BHZRJJOHZFYXTO-UHFFFAOYSA-L 0.000 description 1
- 235000019252 potassium sulphite Nutrition 0.000 description 1
- 125000003226 pyrazolyl group Chemical group 0.000 description 1
- 125000004076 pyridyl group Chemical group 0.000 description 1
- 125000000168 pyrrolyl group Chemical group 0.000 description 1
- 125000002943 quinolinyl group Chemical group N1=C(C=CC2=CC=CC=C12)* 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 230000006798 recombination Effects 0.000 description 1
- 238000005215 recombination Methods 0.000 description 1
- 239000013074 reference sample Substances 0.000 description 1
- 229910052703 rhodium Inorganic materials 0.000 description 1
- 239000010948 rhodium Substances 0.000 description 1
- MHOVAHRLVXNVSD-UHFFFAOYSA-N rhodium atom Chemical compound [Rh] MHOVAHRLVXNVSD-UHFFFAOYSA-N 0.000 description 1
- 238000007142 ring opening reaction Methods 0.000 description 1
- 238000002390 rotary evaporation Methods 0.000 description 1
- 230000035945 sensitivity Effects 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- HBMJWWWQQXIZIP-UHFFFAOYSA-N silicon carbide Chemical class [Si+]#[C-] HBMJWWWQQXIZIP-UHFFFAOYSA-N 0.000 description 1
- LIVNPJMFVYWSIS-UHFFFAOYSA-N silicon monoxide Chemical class [Si-]#[O+] LIVNPJMFVYWSIS-UHFFFAOYSA-N 0.000 description 1
- 229910052709 silver Inorganic materials 0.000 description 1
- 239000004332 silver Substances 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 235000010265 sodium sulphite Nutrition 0.000 description 1
- 239000002689 soil Substances 0.000 description 1
- 239000007784 solid electrolyte Substances 0.000 description 1
- 239000006104 solid solution Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- USPTVMVRNZEXCP-UHFFFAOYSA-N sulfamoyl fluoride Chemical compound NS(F)(=O)=O USPTVMVRNZEXCP-UHFFFAOYSA-N 0.000 description 1
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 238000010345 tape casting Methods 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 125000003831 tetrazolyl group Chemical group 0.000 description 1
- 230000010512 thermal transition Effects 0.000 description 1
- 125000000335 thiazolyl group Chemical group 0.000 description 1
- 125000001544 thienyl group Chemical group 0.000 description 1
- XOLBLPGZBRYERU-UHFFFAOYSA-N tin dioxide Chemical compound O=[Sn]=O XOLBLPGZBRYERU-UHFFFAOYSA-N 0.000 description 1
- 229910001887 tin oxide Inorganic materials 0.000 description 1
- OCDVSJMWGCXRKO-UHFFFAOYSA-N titanium(4+);disulfide Chemical class [S-2].[S-2].[Ti+4] OCDVSJMWGCXRKO-UHFFFAOYSA-N 0.000 description 1
- 229910052723 transition metal Inorganic materials 0.000 description 1
- 125000001425 triazolyl group Chemical group 0.000 description 1
- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 description 1
- 239000010937 tungsten Substances 0.000 description 1
- 229910021642 ultra pure water Inorganic materials 0.000 description 1
- 239000012498 ultrapure water Substances 0.000 description 1
- 238000009827 uniform distribution Methods 0.000 description 1
- 229910052720 vanadium Inorganic materials 0.000 description 1
- GPPXJZIENCGNKB-UHFFFAOYSA-N vanadium Chemical compound [V]#[V] GPPXJZIENCGNKB-UHFFFAOYSA-N 0.000 description 1
- 229910001928 zirconium oxide Inorganic materials 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F214/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen
- C08F214/18—Monomers containing fluorine
- C08F214/26—Tetrafluoroethene
- C08F214/262—Tetrafluoroethene with fluorinated vinyl ethers
-
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- C08F2/00—Processes of polymerisation
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- C08F2/10—Aqueous solvent
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- C08F214/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen
- C08F214/18—Monomers containing fluorine
- C08F214/184—Monomers containing fluorine with fluorinated vinyl ethers
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- C08F8/00—Chemical modification by after-treatment
- C08F8/12—Hydrolysis
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- C08F8/00—Chemical modification by after-treatment
- C08F8/34—Introducing sulfur atoms or sulfur-containing groups
- C08F8/36—Sulfonation; Sulfation
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- C08F8/00—Chemical modification by after-treatment
- C08F8/44—Preparation of metal salts or ammonium salts
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- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J3/00—Processes of treating or compounding macromolecular substances
- C08J3/02—Making solutions, dispersions, lattices or gels by other methods than by solution, emulsion or suspension polymerisation techniques
- C08J3/03—Making solutions, dispersions, lattices or gels by other methods than by solution, emulsion or suspension polymerisation techniques in aqueous media
- C08J3/05—Making solutions, dispersions, lattices or gels by other methods than by solution, emulsion or suspension polymerisation techniques in aqueous media from solid polymers
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- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J5/00—Manufacture of articles or shaped materials containing macromolecular substances
- C08J5/20—Manufacture of shaped structures of ion-exchange resins
- C08J5/22—Films, membranes or diaphragms
- C08J5/2206—Films, membranes or diaphragms based on organic and/or inorganic macromolecular compounds
- C08J5/2218—Synthetic macromolecular compounds
- C08J5/2231—Synthetic macromolecular compounds based on macromolecular compounds obtained by reactions involving unsaturated carbon-to-carbon bonds
- C08J5/2243—Synthetic macromolecular compounds based on macromolecular compounds obtained by reactions involving unsaturated carbon-to-carbon bonds obtained by introduction of active groups capable of ion-exchange into compounds of the type C08J5/2231
- C08J5/225—Synthetic macromolecular compounds based on macromolecular compounds obtained by reactions involving unsaturated carbon-to-carbon bonds obtained by introduction of active groups capable of ion-exchange into compounds of the type C08J5/2231 containing fluorine
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- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D11/00—Inks
- C09D11/52—Electrically conductive inks
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- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D127/00—Coating compositions based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Coating compositions based on derivatives of such polymers
- C09D127/02—Coating compositions based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Coating compositions based on derivatives of such polymers not modified by chemical after-treatment
- C09D127/12—Coating compositions based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Coating compositions based on derivatives of such polymers not modified by chemical after-treatment containing fluorine atoms
- C09D127/18—Homopolymers or copolymers of tetrafluoroethene
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- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
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- C09D127/00—Coating compositions based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Coating compositions based on derivatives of such polymers
- C09D127/22—Coating compositions based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Coating compositions based on derivatives of such polymers modified by chemical after-treatment
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M4/00—Electrodes
- H01M4/86—Inert electrodes with catalytic activity, e.g. for fuel cells
- H01M4/8663—Selection of inactive substances as ingredients for catalytic active masses, e.g. binders, fillers
- H01M4/8668—Binders
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M8/00—Fuel cells; Manufacture thereof
- H01M8/10—Fuel cells with solid electrolytes
- H01M8/1004—Fuel cells with solid electrolytes characterised by membrane-electrode assemblies [MEA]
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- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M8/00—Fuel cells; Manufacture thereof
- H01M8/10—Fuel cells with solid electrolytes
- H01M8/1016—Fuel cells with solid electrolytes characterised by the electrolyte material
- H01M8/1018—Polymeric electrolyte materials
- H01M8/102—Polymeric electrolyte materials characterised by the chemical structure of the main chain of the ion-conducting polymer
- H01M8/1023—Polymeric electrolyte materials characterised by the chemical structure of the main chain of the ion-conducting polymer having only carbon, e.g. polyarylenes, polystyrenes or polybutadiene-styrenes
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M8/00—Fuel cells; Manufacture thereof
- H01M8/10—Fuel cells with solid electrolytes
- H01M8/1016—Fuel cells with solid electrolytes characterised by the electrolyte material
- H01M8/1018—Polymeric electrolyte materials
- H01M8/1039—Polymeric electrolyte materials halogenated, e.g. sulfonated polyvinylidene fluorides
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- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F216/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an alcohol, ether, aldehydo, ketonic, acetal or ketal radical
- C08F216/12—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an alcohol, ether, aldehydo, ketonic, acetal or ketal radical by an ether radical
- C08F216/14—Monomers containing only one unsaturated aliphatic radical
- C08F216/1416—Monomers containing oxygen in addition to the ether oxygen, e.g. allyl glycidyl ether
-
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- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F216/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an alcohol, ether, aldehydo, ketonic, acetal or ketal radical
- C08F216/12—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an alcohol, ether, aldehydo, ketonic, acetal or ketal radical by an ether radical
- C08F216/14—Monomers containing only one unsaturated aliphatic radical
- C08F216/1466—Monomers containing sulfur
- C08F216/1475—Monomers containing sulfur and oxygen
-
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- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F2500/00—Characteristics or properties of obtained polyolefins; Use thereof
- C08F2500/12—Melt flow index or melt flow ratio
-
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- C08F2800/00—Copolymer characterised by the proportions of the comonomers expressed
- C08F2800/10—Copolymer characterised by the proportions of the comonomers expressed as molar percentages
-
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- C08F2810/00—Chemical modification of a polymer
- C08F2810/50—Chemical modification of a polymer wherein the polymer is a copolymer and the modification is taking place only on one or more of the monomers present in minority
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- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2327/00—Characterised by the use of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Derivatives of such polymers
- C08J2327/02—Characterised by the use of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Derivatives of such polymers not modified by chemical after-treatment
- C08J2327/12—Characterised by the use of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Derivatives of such polymers not modified by chemical after-treatment containing fluorine atoms
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- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M8/00—Fuel cells; Manufacture thereof
- H01M8/10—Fuel cells with solid electrolytes
- H01M2008/1095—Fuel cells with polymeric electrolytes
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- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M2300/00—Electrolytes
- H01M2300/0017—Non-aqueous electrolytes
- H01M2300/0065—Solid electrolytes
- H01M2300/0082—Organic polymers
Definitions
- Copolymers of tetrafluoroethylene and polyfluorovinyloxy monomers including sulfonyl fluoride pendant groups have been made. See, for example, U.S. Pat. Nos. 3,282,875 (Connolly), 3,718,627 (Grot), and 4,267,364 (Grot). Copolymers of fluorinated olefins and polyfluoroallyloxy sulfonyl fluorides have been made. See, for example, U.S. Pat. Nos. 4,273,729 (Krespan) and 8,227, 139 (Watakabe), and International Pat. Appl. Pub. No. WO 00/24709 (Farnham et al.). Hydrolysis of the sulfonyl fluoride of these copolymers to form an acid or acid salt provides ionic copolymers, which are also called ionomers.
- Certain recently disclosed ionomers are said to have high oxygen permeability. See, for example, U.S. Pat. Appl. Pub. Nos. 2017/0183435 (Ino), 2013/0253157 (Takami), 2013/0245219 (Perry), and 2013/0252134 (Takami), and U.S. Pat. No. 8,470,943 (Watakabe).
- Electrode catalyst layers including a catalyst (e.g., platinum) and an ionomer. Since the catalysts (e.g., platinum) are typically expensive, decreasing the amount of catalyst can be desirable. For an ionomer used in the electrode, high oxygen permeability is desirable to minimize resistance. In the ionic catalyst layer, it is desirable to have a high oxygen permeability without lowering the ionic conductivity.
- a catalyst e.g., platinum
- ionomer e.g., platinum
- the copolymers of the present disclosure include vinyl ether or allyl ether monomer units in addition to tetrafluoroethylene and sulfonyl group-containing monomer units. Inclusion of such vinyl and allyl ethers can typically provide high oxygen permeation ionomers for electrode applications. The melt flow indexes and equivalent weights of the copolymers typically also provide advantageous mechanical properties and conductivity. Inclusion of vinyl ether and allyl ether monomers can also lead to an improved processability profile in common solvents by improving solubility in a dispersion.
- the present disclosure provides a copolymer including divalent units represented by formula -[CF2-CF2]-, divalent units independently represented by formula:
- a is 0 or 1
- b is a number from 2 to 8
- c is a number from 0 to 2
- e is a number from 1 to 8
- Z is independently a hydrogen, alkyl having up to four carbon atoms, an alkali-metal cation, or a quaternary ammonium cation
- Rf is a linear or branched perfluoroalkyl group having from 1 to 8 carbon atoms and optionally interrupted by one or more -O- groups
- z is 0, 1, or 2
- each n is independently from 1, 2, 3, or 4
- m is 0 or 1.
- Z is hydrogen, the copolymer has an alpha transition temperature of up to 100 ° C.
- the copolymer has an -SO 3 Z equivalent weight in a range from 300 to 1400, and a variation of the copolymer in which -SO 3 Z is replaced with -SO 2 F has a melt flow index of up to 80 grams per ten minutes measured at a temperature of 265 ° C and at a support weight of 5 kg.
- the present disclosure provides a polymer electrolyte membrane that includes the copolymer of the present disclosure.
- the present disclosure provides a catalyst ink that includes the copolymer of the present disclosure.
- the present disclosure provides a membrane electrode assembly that includes at least one of such a polymer electrolyte membrane or catalyst ink.
- the present disclosure provides a binder for an electrochemical system that includes the copolymer of the present disclosure. In another aspect, the present disclosure provides a battery or electrode that includes such a binder.
- the present disclosure provides a copolymer including divalent units represented by formula -[CF2-CF2]-;
- a is 0 or 1
- b is 2 to 8
- c is 0 to 2
- e is 1 to 8
- Rf is a linear or branched perfluoroalkyl group having from 1 to 8 carbon atoms and optionally interrupted by one or more - O- groups
- z is 0, 1, or 2
- each n is independently 1, 2, 3, or 4
- m is 0 or 1.
- the copolymer has an -SO 2 F equivalent weight in a range from 300 to 1400 and a melt flow index of up to 80 grams per ten minutes measured at a temperature of 265 ° C and at a support weight of 5 kg.
- the copolymer has an alpha transition temperature of up to 100 ° C.
- Such copolymers are useful for making the copolymers described above.
- alkyl group and the prefix “alk-” are inclusive of both straight chain and branched chain groups and of cyclic groups. Unless otherwise specified, alkyl groups herein have up to 20 carbon atoms. Cyclic groups can be monocyclic or polycyclic and, in some embodiments, have from 3 to 10 ring carbon atoms.
- aryl and arylene as used herein include carbocyclic aromatic rings or ring systems, for example, having 1, 2, or 3 rings and optionally containing at least one heteroatom (e.g., O, S, or N) in the ring optionally substituted by up to five substituents including one or more alkyl groups having up to 4 carbon atoms (e.g., methyl or ethyl), alkoxy having up to 4 carbon atoms, halo (i.e., fluoro, chloro, bromo or iodo), hydroxy, or nitro groups.
- heteroatom e.g., O, S, or N
- substituents including one or more alkyl groups having up to 4 carbon atoms (e.g., methyl or ethyl), alkoxy having up to 4 carbon atoms, halo (i.e., fluoro, chloro, bromo or iodo), hydroxy, or nitro groups.
- aryl groups include phenyl, naphthyl, biphenyl, fluorenyl as well as furyl, thienyl, pyridyl, quinolinyl, isoquinolinyl, indolyl, isoindolyl, triazolyl, pyrrolyl, tetrazolyl, imidazolyl, pyrazolyl, oxazolyl, and thiazolyl.
- Alkylene is the multivalent (e.g., divalent or trivalent) form of the "alkyl” groups defined above.
- Alkylene is the multivalent (e.g., divalent or trivalent) form of the "aryl” groups defined above.
- Arylalkylene refers to an “alkylene” moiety to which an aryl group is attached.
- Alkylarylene refers to an “arylene” moiety to which an alkyl group is attached.
- perfluoro and “perfluorinated” refer to groups in which all C-H bonds are replaced by C-F bonds.
- -CF2CF2-O-CF2-CF2- is a perfluoroalkylene group interrupted by an -0-.
- the copolymer of the present disclosure includes divalent units represented by formula -[CF2-CF2]-. In some embodiments, the copolymer comprises at least 60 mole % of divalent units represented by formula -[CF2-CF2]-, based on the total moles of divalent units. In some embodiments, the copolymer comprises at least 65, 70, 75, 80, or 90 mole % of divalent units represented by formula
- Divalent units represented by formula -[CF2-CF2]- are incorporated into the copolymer by copolymerizing components including tetrafiuoroethylene (TFE).
- TFE tetrafiuoroethylene
- the components to be polymerized include at least 60, 65, 70, 75, 80, or 90 mole % TFE, based on the total moles of components to be polymerized.
- the copolymer of the present disclosure includes divalent units independently represented by formula:
- a is 0 or 1
- b is a number from 2 to 8
- c is a number from 0 to 2
- e is a number from 1 to 8.
- a is 0; in some embodiments, a is 1.
- b is a number from 2 to 6 or 2 to 4.
- b is 2.
- e is a number from 1 to 6 or 2 to 4.
- e is 2.
- e is 4.
- c is 0 or 1.
- c is 0.
- c is 0, and e is 2 or 4.
- c is 0, and e is 3 to 8, 3 to 6, 3 to 4, or 4.
- each Z is independently a hydrogen, alkyl having up to 4, 3, 2, or 1 carbon atoms, an alkali metal cation, or a quaternary ammonium cation.
- the quaternary ammonium cation can be substituted with any combination of hydrogen and alkyl groups, in some embodiments, alkyl groups independently having from one to four carbon atoms.
- Z is an alkali- metal cation.
- Z is a sodium or lithium cation.
- Z is a sodium cation.
- Copolymers having divalent units represented by this formula can be prepared by copolymerizing components including at least one polyfluoroallyloxy or polyfluorovinyloxy compound represented by formula
- CF2 CF(CF2)a-[0(CF2)b]c-0-(CF2) e -S02X", in which a, b, c, and e are as defined above in any of their embodiments, and each X" is independently -F, -NZH, or -OZ.
- Suitable polyfluoroallyloxy and polyfluorovinyloxy compounds of this formula include
- CF2 CFCF 2 -0-CF2-S0 2 X
- CF 2 CFCF2-0-CF 2 CF2-S02X
- CF 2 CFCF2-0-CF2CF 2 CF2-S02X
- CF 2 CFCF2-0-CF2CF2CF2-S0 2 X
- CF 2 CF-0-CF 2 -S0 2 X
- CF2 CF-0-CF 2 CF2-S0 2 X
- CF 2 CF-0-CF2CF 2 CF2-S02X
- CFz ⁇ F-O-CFzCFzCFzCFz-SOzX
- CF 2 CFCF 2 -[0(CF 2 ) b ] c -0-(CF 2 ) e -S0 2 F
- a base e.g., alkali metal hydroxide or ammonium hydroxide
- CF 2 CFCF 2 -[0(CF 2 ) b ]c-0-(CF 2 ) e -S0 3 Z.
- At least some of the fluorinated divalent units are derived from at least one short-chain S0 2 X"-containing vinyl ether monomer.
- short-chain S0 2 X"-containing vinyl ether monomers may be useful components to be polymerized in the methods according to the present disclosure.
- FC(0)-CF(CF3)-0-(CF 2 ) 2 -S0 2 F As reported in Gronwald, O., et al; "Synthesis of difluoroethyl perfluorosulfonate monomer and its application"; J. Fluorine Chem., 2008, 129, 535- 540, the acid fluoride can be combined with a methanol solution of sodium hydroxide to form the disodium salt, which can be dried and heated in dry diglyme to effect the carboxylation.
- FC(O)- CF(CF3)-0-(CF 2 ) 2 -S0 2 F can be prepared by ring-opening and derivatization of tetrafluoroethane- ⁇ -sultone as described in U.S. Pat. No. 4,962,292 (Marraccini et al.).
- the copolymer includes divalent units independently represented by formula
- Rf is a linear or branched perfluoroalkyl group having from 1 to 8 carbon atoms and optionally interrupted by one or more -
- n is 1, 3, or 4, or from 1 to 3, or from 2 to 3, or from 2 to 4.
- n is 1, 3, or 4.
- n is 1 in any of the formulas described above, for example, n is from 1 to 4, 1 to 3, 2 to 3, or 2 to 4.
- n is 1 or 3.
- n is i .
- n is not 3.
- the n in the two C n F2n groups may be independently selected. However, within a C n F2n group, a person skilled in the art would understand that n is not independently selected.
- C n F2n may be linear or branched. In some embodiments, C n F2n is branched, for example,
- C n F2n can be written as (CF2) n , which refers to a linear perfluoroalkylene group.
- CF2 n refers to a linear perfluoroalkylene group.
- C n F2n is -CF2-CF2- CF 2 -.
- (OC n F2n) z is represented by -0-(CF2)i-4-[0(CF2) i-4]o-i .
- Rf is a linear or branched perfluoroalkyl group having from 1 to 8 (or 1 to 6) carbon atoms that is optionally interrupted by up to 4, 3, or 2 -O- groups.
- Rf is a perfluoroalkyl group having from 1 to 4 carbon atoms optionally interrupted by one -O- group.
- z is 0, m is 0, and Rf is a linear or branched perfluoroalkyl group having from 1 to 4 carbon atoms.
- z is 0, m is 0, and Rf is a branched perfluoroalkyl group having from 3 to 8 carbon atoms. In some embodiments, m is 1, and Rf is a branched perfluoroalkyl group having from 3 to 8 carbon atoms or a linear perfluoroalkyl group having 5 to 8 carbon atoms. In some embodiments, Rf is a branched perfluoroalkyl group having from 3 to 6 or 3 to 4 carbon atoms.
- An example of a useful perfluoroalkyl vinyl ether (PAVE) from which these divalent units in which m and z are 0 are derived is perfluoroisopropyl vinyl ether
- PAVEs include perfluoromethyl vinyl ether, perfluoroethyl vinyl ether, and perfluoropropyl vinyl ether.
- PAOVE perfluoroalkoxyalkyl vinyl ethers
- CF2 CFOCF2CF20CF2CF2CF2CF 2 OCF 3 , CFz ⁇ FOCFzCFzOCFzCFzCFzCFzOCF,
- CF 2 CFOCF2CF2(OCF 2 )30CF 3 ,
- CF 2 CFOCF2CF20CF2CF20CF2CF 2 CF 3
- CF 2 CFOCF 2 CF(CF 3 )-0-C 3 F 7 (PPVE-2)
- the perfluoroalkoxyalkyl vinyl ether is selected from
- CF2 CFOCF 2 CF2(OCF 2 )40CF 3 , and combinations thereof.
- Many of these perfluoroalkoxyalkyl vinyl ethers can be prepared according to the methods described in U.S. Pat. Nos. 6,255,536 (Worm et al.) and 6,294,627 (Worm et al.).
- the PAOVE is perfluoro-3-methoxy-n-propyl vinyl ether.
- the PAOVE is other than perfluoro-3-methoxy-n-propyl vinyl ether.
- CF 2 CFCF20CF2CF2CF 2 OCF 3
- CF 2 CFCF20CF 2 OCF2CF 3
- CF 2 CFCF20CF2CF20CF 2 OCF 3 , CFz ⁇ FCFzOCFzCFzOCFzCFzOCF,
- CF2 CFCF20CF2CF20CF2CF2CF 2 OCF 3 , CFz ⁇ FCFzOCFzCFzOCFzCFzCFzOCF,
- CF2 CFCF20CF2CF20CF2CF2CF 2 OCF 3 , CFz ⁇ FCFzOCFzCFzOCFzCFzCFzOCF,
- perfluoroalkoxyalkyl allyl ethers can be prepared, for example, according to the methods described in U.S. Pat. No. 4,349,650 (Krespan).
- CF2 CF-CF2-OS02CF3, a polyfluorinated compound comprising at least one ketone or carboxylic acid halide or combination thereof, and fluoride ion.
- Polyfluorinated compounds comprising at least one ketone or carboxylic acid halide or combination thereof and fluoride ions can be any of those described, for example, in U.S. Pat. No. 4,349,650 (Krespan).
- hexafluoropropylene HFP
- the reaction of BCI3 and CISO3H can be carried out, for example, by dropwise addition of neat CISO3H to gaseous BCI3 at below 50 °C or, in the case of condensed
- BCI3 at sub-ambient temperature.
- the reaction can be carried out at a temperature of least -20 ° C, -10 ° C, 0 ° C, 10 ° C, or 20 ° C and up to 30 ° C, 40 ° C, or 50 ° C.
- the addition of CISO 3 H to BC1 3 can be carried out at a rate, for example, to maintain the temperature of the mixture at 10 ° C or below.
- B(0S02C1)3 can be isolated as a white powder after volatile starting materials are removed under vacuum. B(0S02C1)3 can then be suspended or dissolved in a solvent, and HFP can be added at below 50 °C, in some embodiments, at sub-ambient temperature.
- the reaction can be carried out at a temperature of least -20 ° C, -10 ° C, 0 ° C, 10 ° C, or 20 ° C and up to 30 ° C, 40 ° C, or 50 ° C.
- Suitable solvents include halogenated solvents (e.g., methylene chloride or Freon-113).
- the solvent is a non-aromatic solvent.
- CF2 CF-CF2-OS02CF3, wherein M is Al or B.
- Al(OS02CF3)3 is commercially available, for example, from chemical suppliers such as abcr GmbH (Karlsruhe, Germany) and Sigma- Aldrich (St. Louis, Missouri). Reaction of BCI3 and CF3SO3H can be useful to provide
- the reaction of BCI3 and CF3SO3H can be carried out, for example, by dropwise addition of neat CF3SO3H to gaseous BCI3 at below 50 °C or, in the case of condensed BCI3 at sub- ambient temperature.
- the reaction can be carried out at a temperature of least -20 ° C, -10 ° C, 0 ° C, 10 ° C, or 20 ° C and up to 30 ° C, 40 ° C, or 50 ° C.
- the addition of CF3SO3H to BCI3 can be carried out at a rate, for example, to maintain the temperature of the mixture at 10 ° C or below.
- B(OS02CF3)3 can be isolated as a white powder after volatile starting materials are removed under vacuum.
- B(OS02CF3)3 can combined with HFP at a temperature above 0 ° C.
- the reaction can be carried out at a temperature up to 50 ° C, 40 ° C, 30 ° C, 20 ° C, or 10 ° C.
- the reaction can be carried out at a temperature in a range from above 0 ° C to 10 ° C, in some embodiments, in a range from 2 ° C to 10 ° C, and in some embodiments, in a range from 4 ° C to 8 ° C.
- the reaction mixture is combined with water at a temperature below 28 ° C, in some embodiments, in a range from above 25 ° C to 27 ° C.
- the reaction product can then be isolated and optionally purified using conventional methods (e.g., separation of the organic fraction, drying over a drying agent, filtering, and distilling).
- the vinyl ethers and allyl ethers described above in any of their embodiments, may be present in the components to be polymerized in any useful amount, in some embodiments, in an amount of up to 20, 15, 10, 7.5, or 5 mole percent, at least 3, 4, 4.5, 5, or 7.5 mole percent, or in a range from 3 to 20, 4 to 20, 4.5 to 20, 5 to 20, 7.5 to 20, or 5 to 15 mole percent, based on the total amount of polymerizable components.
- the copolymer according to the present disclosure can include divalent units derived from these vinyl ethers and allyl ethers in any useful amount, in some embodiments, in an amount of up to 20, 15, 10, 7.5, or 5 mole percent, at least 3, 4, 4.5, 5, or 7.5 mole percent, or in a range from 3 to 20, 4 to 20, 4.5 to 20, 5 to 20, 7.5 to 20, or 5 to 15 mole percent, based on the total moles of divalent units.
- f2 is fluorine or a perfluoroalkyl having from 1 to 8, in some embodiments 1 to 3, carbon atoms, and each R is independently hydrogen, fluorine, or chlorine.
- fluorinated olefins useful as components of the polymerization include, hexafluoropropylene (HFP), trifluorochloroethylene (CTFE), and partially fluorinated olefins (e.g., vinylidene fluoride (VDF), tetrafluoropropylene (R1234yf), pentafluoropropylene, and trifluoroethylene).
- the copolymer includes at least one of divalent units derived from chlorotrifluoroethylene or divalent units derived from hexafluoropropylene.
- Divalent units represented by formula -[CR2-CFRf2]- may be present in the copolymer in any useful amount, in some embodiments, in an amount of up to 10, 7.5, or 5 mole percent, based on the total moles of divalent units.
- the copolymer is essentially free of VDF units, and the components to be copolymerized are essentially free of
- VDF may undergo dehydrofluorination, and it may be useful to exclude VDF from the components to be polymerized.
- Essentially free of VDF can mean that VDF is present in the components to be polymerized at less than 1 (in some
- Copolymers of the present disclosure can comprise divalent units independently represented by formula:
- p is 0 or 1, q is 2 to 8, r is 0 to 2, s is 1 to 8, and Z' is a hydrogen, an alkali-metal cation or a quaternary ammonium cation.
- q is a number from 2 to 6 or 2 to 4.
- q is 2.
- s is a number from 1 to 6 or 2 to 4.
- s is 2.
- s is 4.
- r is 0 or 1.
- r is 0.
- s is 2 or 4.
- q is 3, r is 1, and s is 2.
- C S F2 S may be linear or branched.
- C S F2 S can be written as (CF2)s, which refers to a linear perfluoroalkylene group.
- CF2s refers to a linear perfluoroalkylene group.
- r 2
- the q in the two C q F2 q groups may be independently selected.
- q is not independently selected.
- Each Z' is independently a hydrogen, an alkali metal cation, or a quaternary ammonium cation.
- the quaternary ammonium cation can be substituted with any combination of hydrogen and alkyl groups, in some embodiments, alkyl groups independently having from one to four carbon atoms.
- Z' is an alkali-metal cation.
- Z' is a sodium or lithium cation.
- Z' is a sodium cation.
- copolymer may be present in the copolymer in any useful amount, in some embodiments, in an amount of up to 10, 7.5, or 5 mole percent, based on the total moles of divalent units.
- each of X, Y, and W is independently fluoro, hydrogen, alkyl, alkoxy, polyoxyalkyl, perfluoroalkyl, perfluoroalkoxy or perfluoropolyoxyalkyl
- m and p are independently an integer from 0 to 15, and n, o are independently 0 or 1.
- X, Y, and W are each independently fluoro, CF3, C2F5, C3F7, C4F9, hydrogen, Ct1 ⁇ 4, C2H5, C3H7, C4H9. In some embodiments, X, Y, and W are each fluoro (e.g., as in
- n and o are 1, and the bisolefins are divinyl ethers, diallyl ethers, or vinyl-allyl ethers.
- RF represents linear or branched perfluoroalkylene or perfluoropolyoxyalkylene or arylene, which may be non- fluorinated or fluorinated.
- RF is perfluoroalkylene having from 1 to 12, from 2 to 10, or from 3 to 8 carbon atoms.
- the arylene may have from 5 to 14, 5 to 12, or 6 to 10 carbon atoms and may be non-substituted or substituted with one or more halogens other than fluoro, perfluoroalkyl (e.g. -CF3 and -CF2CF3), perfluoroalkoxy (e.g.
- RF is phenylene or mono-, di-, tri- or tetrafluoro- phenylene, with the ether groups linked in the ortho, para or meta position.
- RF is CF 2 ; (CF 2 ) Q wherein q is 2, 3, 4, 5, 6, 7 or 8; CF 2 -0-CF 2 ; CF 2 -0-CF 2 -CF 2 ; CF(CF 3 )CF 2 ; (CF 2 ) 2 -0-CF(CF3)-CF 2 ; CF(CF3)-CF2-0-CF(CF 3 )CF 2 ; or (CF 2 )2-0-CF(CF3)-CF2-0-CF(CF3)-CF 2 - O-CF2.
- the bisolefins can introduce long chain branches as described in U.S. Pat. Appl. Pub. No. 2010/0311906 (Lavallee et al.).
- bisolefins described above in any of their embodiments, may be present in the components to be polymerized in any useful amount, in some embodiments, in an amount of up to 2, 1, or 0.5 mole percent and in an amount of at least 0.1 mole percent, based on the total amount of polymerizable components.
- Copolymers of the present disclosure can also include units derived from non-fluorinated monomers.
- suitable non-fluorinated monomers include ethylene, propylene, isobutylene, ethyl vinyl ether, vinyl benzoate, ethyl allyl ether, cyclohexyl allyl ether,
- the components to be polymerized further include acrylic acid or methacrylic acid, and the copolymer of the present disclosure includes units derived from acrylic acid or methacrylic acid.
- the copolymer of the present disclosure does not include cyclic structures comprising fluorinated carbon atoms and oxygen atoms in the main chain (that is, divalent units comprising such cyclic structures).
- Hydrolysis of a copolymer having -SO2F groups with an alkaline hydroxide (e.g. LiOH, NaOH, or KOH) solution provides -SO3Z groups, which may be subsequently acidified to SO3H groups.
- Treatment of a copolymer having -SO 2 F groups with water and steam can form SO3H groups.
- copolymers having -SO 2 F groups that is, in which X" is F
- Z is an alkali-metal cation.
- Z is a sodium or lithium cation.
- Z is a sodium cation.
- the copolymer of the present disclosure can have an -SO3Z equivalent weight of up to 1400, 1300, 1200, 1100, or 1000. In some embodiments, the copolymer has an -SO3Z equivalent weight of at least 300, 400, or 500. In some embodiments, the copolymer has an -SO3Z equivalent weight in a range from 300 to 1400, 300 to 1300, 300 to 1200, 400 to 1200, or 400 to 1000. In general, the -SO3Z equivalent weight of the copolymer refers to the weight of the copolymer containing one mole of -SO3Z groups, wherein Z is as defined above in any of its embodiments.
- the -SO3Z equivalent weight of the copolymer refers to the weight of the copolymer that will neutralize one equivalent of base. In some embodiments, the -SO3Z equivalent weight of the copolymer refers to the weight of the copolymer containing one mole of sulfonate groups (i.e., -SO3 " ). Decreasing the -SO3Z equivalent weight of the copolymer tends to increase proton conductivity in the copolymer but tends to decrease its crystallinity, which may compromise the mechanical properties of the copolymer (e.g., tensile strength).
- the -SO3Z equivalent weight of the copolymer of the present disclosure typically and advantageously provides a balance of the requirements for the electrical and mechanical properties of the copolymer.
- Equivalent weight can be calculated from the molar ratio of monomer units in the copolymer using, for example, the equation shown in the Examples, below.
- the copolymer of the present disclosure can have up to 30 mole percent of divalent units represented by formula , based on the total amount of the divalent units. In some embodiments, the copolymer comprises up to 25 or 20 mole percent of these divalent units, based on the total amount of these divalent units.
- CF2 CF(CF2)a-(OCbF2b)c-0-(C e F2e)-S02X", based on the total amount of components that are copolymerized.
- the molecular weights of copolymers of the present disclosure can be characterized by the melt viscosity or the melt flow index (MFI, e.g., 265 ° C/5 kg) of a variation of the copolymer in which -SO3Z is replaced with -SO 2 F.
- MFI melt viscosity or the melt flow index
- the copolymer of the present disclosure has an MFI of up to 80 grams per 10 minutes, 70 grams per 10 minutes, 60 grams per 10 minutes, 50 grams per 10 minutes, up to 40 grams per 10 minutes, 30 grams per 10 minutes, or 20 grams per 10 minutes.
- the copolymer of the present disclosure has an MFI of up to 15 grams per 10 minutes or up to 12 grams per 10 minutes.
- the copolymer can be adjusted to have an MFI of up to 80 grams per 10 minutes by adjusting the amount of the initiator and/or chain-transfer agent used during polymerization, both of which affect the molecular weight and molecular-weight distribution of the copolymer. MFI can also be controlled by the rate of addition of initiator to the polymerization. Variations in the monomer composition can also affect the MFI. For the purposes of the present disclosure, MFI is measured according to the test method described in the Examples, below.
- an MFI of about 20 grams per 10 minutes measured at 270 " C/2.16 kg will give an MFI of 43 grams per 10 minutes measured at 265 ° C/5 kg.
- an MFI is measured at 265 ° C/5 kg, a value of more than twice than an MFI measured at 270 " C/2.16 kg is obtained.
- Copolymers of the present disclosure are generally considered ionomers.
- Ionomers typically exhibit a thermal transition between a state in which the ionic clusters are closely associated and a state in which the interactions between those clusters have been weakened. This transition is described as an alpha transition, and the transition temperature is T(a). Ionomers with higher T(a) typically have greater mechanical integrity at elevated temperatures than
- the ⁇ -dispersion temperature [T(a)] of copolymer of the present disclosure is up to 110 ° C, 105 ° C, or 100 ° C, or less than 100 ° C, in some embodiments, up to 99.5 ° C or 99 ° C.
- the ⁇ -dispersion temperature [T(a)] of copolymer of the present disclosure is at least room temperature (e.g., 25 ° C), in some embodiments, at least 60 ° C, 65 ° C, 70 ° C, 75 ° C, 80 ° C, 85 ° C, 90 ° C, or 95 ° C. In some embodiments, the ⁇ -dispersion temperature [T(a)] of copolymer of the present disclosure is in a range from 60 ° C to 100 ° C, 70 ° C to 100 ° C, 80 ° C to 100 ° C, 90 ° C to 100 ° C, or 95 ° C to 100 ° C.
- the ⁇ -dispersion temperature [T(a)] of copolymer of the present disclosure is in a range from 60 ° C to 99.5 ° C, 70 ° C to 99.5 ° C, 80 ° C to 99.5 ° C, 90 ° C to 99.5 ° C, or 95 ° C to 99.5 ° C. In some embodiments, the ⁇ -dispersion temperature [T(a)] of copolymer of the present disclosure is in a range from 60 ° C to 99 ° C, 70 ° C to 99 ° C, 80 ° C to 99 ° C, 90 ° C to 99 ° C, or 95 ° C to 99 ° C.
- T(a) various factors can affect the [T(a)].
- a, b, c, and e are selected to provide greater than 2, at least 3, or at least 4 carbon atoms in the side chain of the sulfonyl-substituted divalent units a T(a) up to 100 ° C (e.g., in a range from 80 ° C to 100 ° C, 90 ° C to 100 ° C, or 95 ° C to 100 ° C) may be achieved.
- m, n, z, and Rf are selected to provide greater than 2, at least 3, or at least 4 carbon atoms and at least one or 2 oxygen atoms in the side chain of the divalent units represented by formula
- a T(a) up to 100 ° C (e.g., in a range from 80 ° C to 100 ° C, 90 ° C to 100 ° C, or 95 ° C to 100 ° C) may be achieved. Including more than 3, 4, 4.5, 5, or 7.5 mol percent of these divalent units can be useful for achieving a T(a) in these ranges.
- the cation present in the ionomer affects the T(a).
- T(a) in the copolymer of the present disclosure can be changed, for example, by ion exchange.
- Dynamic mechanical analysis is a useful tool for measuring T(a), as polymer physical property changes accompany this transition.
- the DMA sample cell may be set up in torsion, compression, or tension.
- T(a) is measured by the method described in the Examples, below. Since the T(a) changes with different cations, for the purposes of this disclosure, the T(a) is understood to be the T(a) when Z is hydrogen.
- the glass transition temperature (Tg) is typically defined as the temperature at which an amorphous polymer or amorphous region within a polymer transitions from a glassy material (below Tg) to a rubbery one (above Tg).
- Gas diffusion rates are correlated to free volume in a polymer [see, for example, Diffusion in Polymers, Marcel Dekker (New York), 1996, edited by P. Neogi].
- the free volume increases with temperature, particularly so above the Tg of the polymer.
- the molecular transport of a gas is enhanced the more the temperature of operation exceeds the Tg of the polymer.
- polymers having a relatively low Tg can be desirable for applications in which gas diffusion is required.
- a, b, c, and e may be selected to provide greater than 2, at least 3, or at least 4 carbon atoms in the side chain of the sulfonyl-substituted divalent units to achieve a lower Tg.
- the variation of the copolymer in which -SO3Z is replaced with -SO2F has a Tg less than 30 ° C, less than room temperature, or up to 25 ° C, 20 ° C, 15 ° C, or 10 ° C. Since multiple bulk physical properties of the polymer are different in the glassy state relative to the rubbery state, a variety of methods can be used to measure the Tg.
- DSC Differential scanning calorimetry
- DMA dynamic mechanic analysis
- Tg is measured by the method described in the Examples, below.
- High oxygen permeability in the copolymers disclosed herein can be useful to improve the efficiency of fuel cells, for example.
- Copolymers of the present disclosure typically have useful oxygen permeabilities for fuel cell applications.
- Oxygen permeability can be measured by methods known in the art including the time lag method described in the Examples, below. As shown in comparison of Example 1 and Comparative Example A below, the addition of the divalent unit represented by formula
- Comparable can mean similar to the copolymer of the present disclosure in equivalent weight.
- z is 1 or 2
- the methods of making the copolymer can be carried out by free-radical polymerization.
- the methods of making the copolymer disclosed herein includes radical aqueous emulsion polymerization.
- a water-soluble initiator e.g., potassium permanganate or a peroxy sulfuric acid salt
- a water-soluble initiator e.g., potassium permanganate or a peroxy sulfuric acid salt
- Salts of peroxy sulfuric acid such as ammonium persulfate or potassium persulfate
- a reducing agent such as bisulfites or sulfinates (e.g., fluorinated sulfinates disclosed in U.S. Pat. Nos. 5,285,002 and 5,378,782, both to Grootaert) or the sodium salt of hydroxy methane sulfinic acid (sold under the trade designation "PvONGALIT", BASF Chemical Company, New Jersey, USA).
- the choice of initiator and reducing agent if present, will affect the end groups of the copolymer.
- the concentration range for the initiators and reducing agent can vary from 0.001% to 5% by weight based on the aqueous polymerization medium.
- -SO2X" end groups are introduced in the copolymers according to the present disclosure by generating S03 ⁇ radicals during the polymerization process.
- a sulfite or bisulfite salt e.g., sodium sulfite or potassium sulfite
- SC>3 _ radicals are generated during the polymerization process, resulting in -SC>3 _ end groups. It might be useful to add metal ions to catalyze or accelerate the formation of -SO3 " radicals.
- Buffers include phosphate, acetate, or carbonate (e.g., (NtL ⁇ CCb or NaHCC ) buffers or any other acid or base, such as ammonia or alkali-metal hydroxides.
- the copolymerizing is carried out at a pH of at least 8, higher than 8, at least 8.5, or at least 9.
- the concentration range for the initiators and buffers can vary from 0.01% to 5% by weight based on the aqueous polymerization medium.
- ammonia is added to the reaction mixture in an amount to adjust the pH to at least 8, higher than 8, at least 8.5, or at least 9.
- Typical chain-transfer agents like 3 ⁇ 4, lower alkanes, alcohols, ethers, esters, and CH2CI2 may be useful in the preparation of the copolymer and ionomer according to the present disclosure. Termination primarily via chain-transfer results in a polydispersity of about 2.5 or less. In some embodiments of the method according to the present disclosure, the polymerization is carried out without any chain-transfer agents. A lower polydispersity can sometimes be achieved in the absence of chain-transfer agents. Recombination typically leads to a polydispersity of about 1.5 for small conversions.
- Useful polymerization temperatures can range from 20 ° C to 150 ° C. Typically, polymerization is carried out in a temperature range from 30 ° C to 120 ° C, 40 ° C to 100 ° C, or 50 ° C to 90 ° C.
- the polymerization pressure is usually in the range of 0.4 MPa to 2.5 MPa, 0.6 to 1.8 MPa, 0.8 MPa to 1.5 MPa, and in some embodiments is in the range from 1.0 MPa to 2.0 MPa.
- Fluorinated monomers such as HFP can be precharged and fed into the reactor as described, for example, m Modern Fluoropolymers , ed. John Scheirs, Wiley & Sons, 1997, p. 241.
- perfluoroalkoxyalkyl allyl ethers represented by formula wherein n, z, and Rf are as defined above in any of their embodiments, are typically liquids and may be sprayed into the reactor or added directly, vaporized, or atomized.
- the polymerization process may be conducted with no emulsifier (e.g., no fluorinated emulsifier).
- no emulsifier e.g., no fluorinated emulsifier
- CF2 CF(CF2)a-[0(CF2)b]c-0-(CF2) e -S02X" and the non-functional comonomers (e.g.,
- perfluoroalkoxyalkyl vinyl or perfluoroalkoxyalkyl allyl ethers or bisolefins as a homogenous mixture to the polymerization.
- it is possible to hydrolyze some of the CF 2 CF(CF 2 )a-[0(CF 2 ) b ]c-0-(CF 2 ) e -S0 2 F (e.g., up to 5 ppm) to obtain an "in situ"-emulsifier.
- this method may be conducted in the absence of any other fluorinated emulsifiers. In some embodiments, however, perfluorinated or partially fluorinated emulsifiers may be useful.
- fluorinated emulsifiers are present in a range from about 0.02% to about 3% by weight with respect to the polymer.
- Polymer particles produced with a fluorinated emulsifier typically have an average diameter, as determined by dynamic light scattering techniques, in range of about 10 nanometers (nm) to about 500 nm, and in some embodiments in range of about 50 nm to about 300 nm.
- suitable emulsifiers include perfluorinated and partially fluorinated emulsifier having the formula
- suitable emulsifiers also include perfluorinated polyether emulsifiers having the formula CF3-(OCF2) x -0-CF2-X', wherein x has a value of 1 to 6 and X' represents a carboxylic acid group or salt thereof, and the formula CF3-0-(CF2)3-(OCF(CF3)- CF2) y -0-L-Y' wherein y has a value of 0, 1, 2 or 3, L represents a divalent linking group selected from -CF(CF3)-, -CF2-, and-CF2CF2-, and Y' represents a carboxylic acid group or salt thereof.
- Other suitable emulsifiers include perfluorinated polyether emulsifiers having the formula
- Rf-0(CF2CF20) x CF2COOA wherein Rf is CbFpb+i); where b is 1 to 4, A is a hydrogen atom, an alkali metal or NH4, and x is an integer of from 1 to 3.
- Suitable emulsifiers also include perfluorinated emulsifiers having the formula F(CF2) b O(CF2CF20) x CF2COOA wherein A is a hydrogen atom, an alkali metal or NH4, b is an integer of from 3 to 10, and x is 0 or an integer of from 1 to 3.
- F(CF2) b O(CF2CF20) x CF2COOA perfluorinated emulsifiers having the formula F(CF2) b O(CF2CF20) x CF2COOA wherein A is a hydrogen atom, an alkali metal or NH4, b is an integer of from 3 to 10, and x is 0 or an integer of from 1 to 3.
- Further suitable emulsifiers include fluorinated polyether emulsifiers as described in U.S. Pat. No. 6,429,258 to Morgan et al.
- Suitable emulsifiers also include partially fluorinated polyether emulsifiers having the formula [Rf-(0) t -CHF-(CF2) x -COO-]iX 1+ wherein Rf represents a partially or fully fluorinated aliphatic group optionally interrupted with one or more oxygen atoms, t is 0 or 1 and x is 0 or 1, X 1+ represents a cation having a valence i and i is 1, 2 or 3. (See, e.g., U.S. Pat. Publ. No. 2007/0142541 to Hintzer et al).
- emulsifiers include perfluorinated or partially fluorinated ether-containing emulsifiers as described in U.S. Pat. Publ. Nos. 2006/0223924, 2007/0060699, and 2007/0142513 each to Tsuda et al. and 2006/0281946 to Morita et al.
- Fluoroalkyl for example, perfluoroalkyl carboxylic acids and salts thereof having 6-20 carbon atoms, such as ammonium perfluorooctanoate (APFO) and ammonium perfluorononanoate (see, e.g., U.S. Pat. No. 2,559,752 to Berry) may also be useful.
- APFO ammonium perfluorooctanoate
- U.S. Pat. No. 2,559,752 to Berry ammonium perfluorononanoate
- the method of making the copolymer according to the present disclosure may be conducted in the absence of any of these emulsifiers or any combination thereof.
- the emulsifiers can be removed or recycled from the fluoropolymer latex, if desired, as described in U.S. Pat. Nos. 5,442,097 to Obermeier et al., 6,613,941 to Felix et al., 6,794,550 to Hintzer et al, 6,706,193 to Burkard et al., and 7,018,541 to Hintzer et al.
- the obtained copolymer latices are purified by at least one of anion- or cation-exchange processes to remove functional comonomers, anions, and/or cations before coagulation
- purify refers to at least partially removing impurities, regardless of whether the removal is complete.
- Anionic species that may constitute impurities include, for example, fluoride, anionic residues from surfactants and emulsifiers (e.g., perfluorooctanoate), and residual compounds represented by formula
- CF2 CF(CF2)a-[0(CF2) b ]c-0-(CF2) e -S03 . It should be noted, however, that it may be desirable to not remove ionic fluoropolymer from the dispersion.
- Useful anion exchange resins typically comprise a polymer (typically crosslinked) that has a plurality of cationic groups (e.g., quaternary alkyl ammonium groups) paired with various anions (e.g., halide or hydroxide). Upon contact with the fluoropolymer dispersion, anionic impurities in the dispersion become associated with the anion exchange resin.
- the resultant anion-exchanged dispersion is separated from the anion exchange resin, for example, by filtration. It was reported in U.S. Pat. No. 7,304,101 (Hintzer et al.) that the anionic hydrolyzed fluoropolymer does not appreciably become immobilized on the anion exchange resin, which would lead to coagulation and/or material loss.
- Anionic exchange resins are available commercially from a variety of sources. If the anion exchange resin is not in the hydroxide form it may be at least partially or fully converted to the hydroxide salt form before use. This is typically done by treating the anion exchange resin with an aqueous ammonia or sodium hydroxide solution. Typically, better yields are obtained using gel- type anion-exchange resins than with macroporous anion exchange resins.
- Examples of cationic impurities resulting from the abovementioned polymerization include one or more of, alkali metal cation(s) (e.g., Li + , Na + , K + ), ammonium, quaternary alkyl ammonium, alkaline earth cations (e.g., Mg 2+ , Ca 2+ ), manganese cations (e.g. Mn 2+ ), and Group III metal cations.
- Useful cation exchange resins include polymers (typically cross-linked) that have a plurality of pendant anionic or acidic groups such as, for example, polysulfonates or polysulfonic acids, polycarboxylates or polycarboxylic acids.
- sulfonic acid cation exchange resins examples include sulfonated styrene-divinylbenzene copolymers, sulfonated crosslinked styrene polymers, phenol-formaldehyde -sulfonic acid resins, and benzene-formaldehyde-sulfonic acid resins.
- Carboxylic acid cation exchange resin is an organic acid, cation exchange resin, such as carboxylic acid cation exchange resin.
- Cation exchange resins are available commercially from a variety of sources. Cation exchange resins are commonly supplied commercially in either their acid or their sodium form.
- the cation exchange resin is not in the acid form (i.e., protonated form) it may be at least partially or fully converted to the acid form in order to avoid the generally undesired introduction of other cations into the dispersion.
- This conversion to the acid form may be accomplished by means well known in the art, for example by treatment with any adequately strong acid.
- the anion exchange resin and cation exchange resin may be used individually or in combination as, for example, in the case of a mixed resin bed having both anion and cation exchange resins.
- any coagulant which is commonly used for coagulation of a fluoropolymer latex may be used, and it may, for example, be a water-soluble salt (e.g., calcium chloride, magnesium chloride, aluminum chloride or aluminum nitrate), an acid (e.g., nitric acid, hydrochloric acid or sulfuric acid), or a water-soluble organic liquid (e.g., alcohol or acetone).
- the amount of the coagulant to be added may be in a range of 0.001 to 20 parts by mass, for example, in a range of 0.01 to 10 parts by mass per 100 parts by mass of the latex.
- the latex may be frozen for coagulation or mechanically coagulated, for example, with a homogenizer as described in U.S. Pat. No. 5,463,021 (Beyer et al.).
- the latex may be coagulated by adding poly cations. It may also be useful to avoid acids and alkaline earth metal salts as coagulants to avoid metal contaminants. To avoid coagulation altogether and any contaminants from coagulants, spray drying the latex after polymerization and optional ion-exchange purification may be useful to provide solid copolymer.
- a coagulated copolymer can be collected by filtration and washed with water.
- the washing water may, for example, be ion-exchanged water, pure water, or ultrapure water.
- the amount of the washing water may be from 1 to 5 times by mass to the copolymer or ionomer, whereby the amount of the emulsifier attached to the copolymer can be sufficiently reduced by one washing.
- the copolymer produced can have less than 50 ppm metal ion content, in some embodiments, less than 25 ppm, less than 10 ppm, less than 5 ppm, or less than 1 ppm metal ion content.
- metal ions such as alkali metals, alkaline earth metal, heavy metals (e.g., nickel, cobalt, manganese, cadmium, and iron) can be reduced.
- polymerization can be conducted in the absence of added metal ions.
- potassium persulfate a common alternative initiator or co-initiator with ammonium persulfate
- mechanical and freeze coagulation described above may be used instead of coagulation with metal salts.
- organic initiators as disclosed in U.S. Pat. No. 5,182,342 (Feiring et al.).
- ion exchange can be used, as described above, and the water for polymerization and washing may be deionized.
- the metal ion content of the copolymer can be measured by flame atomic absorption spectrometry after combusting the copolymer and dissolving the residue in an acidic aqueous solution.
- the lower detection limit is less than 1 ppm.
- radical polymerization also can be carried out by suspension polymerization.
- Suspension polymerization will typically produce particle sizes up to several millimeters.
- This method can conveniently eliminate the steps of isolating solid polymer and hydrolyzing, resulting in a more efficient and cost-effective process.
- CF2 CF(CF2) a -[0(CF2)b] c -0-
- each of a, b, c, e, and Z may be independently selected.
- each Z is independently an alkali-metal cation or a quaternary ammonium cation.
- substantially free of compounds represented by formula CF2 CF(CF2) a -[0(CF2)b] c -0- (CF2) e -S02F.
- a copolymer of the present disclosure can be made by
- Fluoropolymers obtained by aqueous emulsion polymerization with inorganic initiators typically have a high number of unstable carbon-based end groups (e.g. more than 200 -COOM or -COF end groups per 10 6 carbon atoms, wherein M is hydrogen, a metal cation, or Nth).
- inorganic initiators e.g. persulfates, KMn04, etc.
- M is hydrogen, a metal cation, or Nth.
- fluorinated ionomers useful for example, in an electrochemical cell, the effect naturally increases as sulfonate equivalent weight decreases. These carbonyl end groups are vulnerable to peroxide radical attacks, which reduce the oxidative stability of the fluorinated ionomers.
- peroxides can be formed. This degrades the fluorinated ionomers, and correspondingly reduces the operational life of the given electrolyte membrane.
- the copolymer of the present disclosure can have up to 400 -COOM and - COF end groups per 10 6 carbon atoms, wherein M is independently an alkyl group, a hydrogen atom, a metallic cation, or a quaternary ammonium cation.
- M is independently an alkyl group, a hydrogen atom, a metallic cation, or a quaternary ammonium cation.
- the copolymer according to the present disclosure has up to 200 unstable end groups per 10 6 carbon atoms.
- the unstable end groups are -COOM or -COF groups, wherein M is an alkyl group, a hydrogen atom, a metallic cation, or a quaternary ammonium cation.
- the copolymer has up to 150, 100, 75, 50, 40, 30, 25, 20, 15, or 10 unstable end groups per 10 6 carbon atoms.
- the number of unstable end groups can be determined by Fourier- transform infrared spectroscopy using the method described below.
- the copolymer according to the present disclosure has up to 50 (in some embodiments, up to 40, 30, 25, 20, 15, or 10) unstable end groups per 10 6 carbon atoms, as polymerized.
- Copolymers according to some embodiments of the present disclosure have -SO2X" end groups.
- -SO2X" end groups can be introduced in the copolymers according to the present disclosure by generating S03 ⁇ radicals during the polymerization process.
- reducing the number of unstable end groups can be accomplished by carrying out the polymerization in the methods disclosed above in the presence of a salt or pseudohalogen as described in U.S. Pat. No. 7,214,740 (Lochhaas et al.).
- Suitable salts can include a chloride anion, a bromide anion, an iodide anion, or a cyanide anion and a sodium, potassium, or ammonium cation.
- the salt used in the free-radical polymerization may be a homogenous salt or a blend of different salts. Examples of useful pseudohalogens are nitrile- containing compounds, which provide nitrile end groups.
- Pseudohalogen nitrile-containing compounds have one or more nitrile groups and function in the same manner as compounds in which the nitrile groups are replaced with a halogen.
- suitable pseudohalogen nitrile- containing compounds include NC-CN, NC-S-S-CN, NCS-CN, Cl-CN, Br-CN,
- I-CN, NCN NCN, and combinations thereof.
- the reactive atoms/groups of the salts or the nitrile groups of the pseudohalogens chemically bond to at least one end of the backbone chain of the fluoropolymer.
- This provides CF2Y 1 end groups instead of carbonyl end groups, wherein Y 1 is chloro, bromo, iodo, or nitrile.
- a KC1 salt at least one of the end groups provided would be a -CF2CI end group.
- the free-radical polymerization is performed in the presence of a NC-CN pseudohalogen, at least one of the end groups provided would be a -CF2CN end group.
- Post-fluorination with fluorine gas can also be used to cope with unstable end groups and any concomitant degradation.
- the post-fluorination may be carried out in any convenient manner.
- the post-fluorination can be conveniently carried out with nitrogen/fluorine gas mixtures in ratios of 75 - 90 : 25 - 10 at temperatures between 20 °C and 250 °C, in some embodiments in a range of 150 °C to 250 °C or 70 °C to 120 °C, and pressures from 10 KPa to 1000 KPa. Reaction times can range from about four hours to about 16 hours. Under these conditions, most unstable carbon-based end groups are removed, whereas -SO2X groups mostly survive and are converted to -SO2F groups.
- post-fluorination is not carried out when non-fluorinated monomers described above are used as monomers in the polymerization or when the copolymer according to the present disclosure includes divalent units independently represented by formula:
- the groups Y 1 in the end groups -CF2Y 1 , described above, are reactive to fluorine gas, which reduces the time and energy required to post-fluorinate the copolymers in these
- a technique that can be useful for dispersing a fluoropolymer in a desired medium is up -concentration of a dilute dispersion of fluoropolymer.
- U.S. Pat. Appl. Pub. Nos. 2017/0183435 reports preparing a fluoropolymer electrolyte solution by heating a solid fluoropolymer electrolyte in a solution of 50% by weight solution of ethanol in water in an autoclave at 160 ° C with stirring for five hours to achieve a fluoropolymer electrolyte solution with a solids concentration of 5% by weight. Concentration under reduced pressure provided a fluoropolymer electrolyte solution with a solids concentration of 20% by weight.
- the copolymer disclosed herein can typically be directly dispersed at a concentration of at least 10, 15, 20, or 25 percent by weight in a solution of water and organic solvent without the need for up-concentrating.
- the copolymer disclosed herein can be directly dispersed at a concentration of up to 30, 40, or 50 percent by weight in a solution of water and organic solvent without the need for up -concentrating.
- a useful method includes combining components comprising water, an organic solvent, and at least ten percent by weight of the copolymer of the present disclosure, based on the total weight of the components, and mixing the components at ambient temperature and pressure to make a fluoropolymer dispersion.
- combining components comprising at least ten percent by weight of the copolymer, based on the total weight of the components refers to the concentration of the copolymer when the components are initially combined (e.g., when organic solvent is first added to an aqueous dispersion of the fluoropolymer) before any agitation of the combined components.
- X is OZ
- Z is hydrogen.
- suitable organic solvents useful for preparing fluoropolymer dispersions of the copolymer of the present disclosure include, lower alcohols (e.g., methanol, ethanol, isopropanol, n-propanol), polyols (e.g., ethylene glycol, propylene glycol, glycerol), ethers (e.g.,
- tetrahydrofuran and dioxane diglyme, polyglycol ethers, ether acetates, acetonitrile, acetone, dimethylsulfoxide (DMSO), N,N dimethyacetamide (DMA), ethylene carbonate, propylene carbonate, dimethylcarbonate, diethylcarbonate, N,N-dimethylformamide (DMF), N- methylpyrrolidinone (NMP), dimethylimidazolidinone, butyrolactone, hexamethylphosphoric triamide (HMPT), isobutyl methyl ketone, sulfolane, and combinations thereof.
- DMSO dimethylsulfoxide
- DMA dimethyacetamide
- DMF N,N-dimethylformamide
- NMP N- methylpyrrolidinone
- HMPT hexamethylphosphoric triamide
- HMPT hexamethylphosphoric triamide
- the copolymer, water, and organic solvent can be heated at a pressure of up to 0.2 MPa or 0.15 MPa at a temperature of up to 100 ° C, 90 ° C, 80 ° C, 70 ° C, 60 ° C, 50 ° C, or 40 ° C.
- the fluoropolymer dispersion may also be made at ambient temperature and pressure.
- the copoylmer of the present disclosure may be useful, for example, in the manufacture of catalyst ink and polymer electrolyte membranes for use in fuel cells or other electrolytic cells.
- a membrane electrode assembly (MEA) is the central element of a proton exchange membrane fuel cell, such as a hydrogen fuel cell.
- Fuel cells are electrochemical cells which produce usable electricity by the catalyzed combination of a fuel such as hydrogen and an oxidant such as oxygen.
- Typical MEA's comprise a polymer electrolyte membrane (PEM) (also known as an ion conductive membrane (ICM)), which functions as a solid electrolyte.
- PEM polymer electrolyte membrane
- ICM ion conductive membrane
- Each electrode layer includes electrochemical catalysts, typically including platinum metal.
- Gas diffusion layers (GDL's) facilitate gas transport to and from the anode and cathode electrode materials and conduct electrical current.
- the GDL may also be called a fluid transport layer (FTL) or a diffuser/current collector (DCC).
- FTL fluid transport layer
- DCC diffuser/current collector
- the anode and cathode electrode layers may be applied to GDL's in the form of a catalyst ink, and the resulting coated GDL's sandwiched with a PEM to form a five-layer MEA.
- the anode and cathode electrode layers may be applied to opposite sides of the PEM in the form of a catalyst ink, and the resulting catalyst-coated membrane (CCM) sandwiched with two GDL's to form a five-layer MEA.
- CCM catalyst-coated membrane
- protons are formed at the anode via hydrogen oxidation and transported across the PEM to the cathode to react with oxygen, causing electrical current to flow in an external circuit connecting the electrodes.
- the PEM forms a durable, non-porous, electrically non-conductive mechanical barrier between the reactant gases, yet it also passes H + ions readily.
- the copolymer of the present disclosure may be useful as and/or useful for making a catalyst ink composition.
- the copolymer e.g., as a component of the fluoropolymer dispersion described above
- catalyst particles e.g., metal particles or carbon-supported metal particles.
- a variety of catalysts may be useful.
- carbon-supported catalyst particles are used. Typical carbon-supported catalyst particles are 50% to 90% carbon and 10% to 50% catalyst metal by weight, the catalyst metal typically comprising platinum for the cathode and platinum and ruthenium in a weight ratio of 2: 1 for the anode.
- catalyst may be applied to the PEM by any suitable means, including both hand and machine methods, including hand brushing, notch bar coating, fluid bearing die coating, wire-wound rod coating, fluid bearing coating, slot-fed knife coating, three-roll coating, or decal transfer. Coating may be achieved in one application or in multiple applications.
- copolymers according to the present disclosure may be useful for making a catalyst layer with one coating application.
- the catalyst ink may be applied to a PEM or a GDL directly, or the catalyst ink may be applied to a transfer substrate, dried, and thereafter applied to the PEM or to the FTL as a decal.
- the catalyst ink includes the copolymer disclosed herein at a concentration of at least 10, 15, or 20 percent by weight and up to 30 percent by weight, based on the total weight of the catalyst ink.
- the catalyst ink includes the catalyst particles in an amount of at least 10, 15, or 20 percent by weight and up to 50, 40, or 30 percent by weight, based on the total weight of the catalyst ink.
- the catalyst particles may be added to the fluoropolymer dispersion made as described above in any of its embodiments.
- the resulting catalyst ink may be mixed, for example, with heating.
- the percent solid in the catalyst ink may be selected, for example, to obtain desirable rheological properties.
- suitable organic solvents useful for including in the catalyst ink include, lower alcohols (e.g., methanol, ethanol, isopropanol, n-propanol), polyols (e.g., ethylene glycol, propylene glycol, glycerol), ethers (e.g., tetrahydrofuran and dioxane), diglyme, polyglycol ethers, ether acetates, acetonitrile, acetone, dimethylsulfoxide (DMSO), N,N dimethyacetamide (DMA), ethylene carbonate, propylene carbonate, dimethylcarbonate, diethylcarbonate, N,N-dimethylformamide (DMF), N- methylpyrrolidinone (NMP), dimethylimidazolidinone, butyrolactone, hexamethylphosphoric triamide (HMPT), isobutyl methyl ketone, sulfolane, and combinations thereof.
- lower alcohols
- the copolymer of the present disclosure may be useful for making a polymer electrolyte membrane.
- the copolymer may be formed into a polymer electrolyte membrane by any suitable method, including casting, molding, and extrusion.
- the membrane is cast from a fluoropolymer dispersion (e.g., those described above in any of their embodiments) and then dried, annealed, or both.
- the copolymer may be cast from a suspension. Any suitable casting method may be used, including bar coating, spray coating, slit coating, and brush coating.
- the membrane may be annealed, typically at a temperature of 120 ° C or higher, more typically 130 " C or higher, most typically 150 ° C or higher.
- a polymer electrolyte membrane can be obtained by obtaining the copolymer in a fluoropolymer dispersion, optionally purifying the dispersion by ion-exchange purification, and concentrating the dispersion to make a membrane.
- the concentration of copolymer is advantageously high (e.g., at least 20, 30, or 40 percent by weight).
- a water-miscible organic solvent is added to facilitate film formation.
- water-miscible solvents include, lower alcohols (e.g., methanol, ethanol, isopropanol, n-propanol), polyols (e.g., ethylene glycol, propylene glycol, glycerol), ethers (e.g., tetrahydrofuran and dioxane), ether acetates, acetonitrile, acetone, dimethylsulfoxide (DMSO), N,N dimethyacetamide (DMA), ethylene carbonate, propylene carbonate, dimethylcarbonate, diethylcarbonate, ⁇ , ⁇ -dimethylformamide (DMF), N- methylpyrrolidinone (NMP), dimethylimidazolidinone, butyrolactone, hexamethylphosphoric triamide (HMPT), isobutyl methyl ketone, sulfolane, and combinations thereof.
- lower alcohols e.g., methanol, ethanol, iso
- the present disclosure provides a membrane electrode assembly comprising at least one of a catalyst ink comprising the copolymer of the present disclosure or a polymer electrolyte membrane comprising the copolymer of the present disclosure.
- the polymer electrolyte membrane and catalyst ink use embodiments of the copolymer disclosed herein.
- the catalyst ink and polymer electrolyte membrane may use the same or different copolymers.
- the catalyst ink comprises the copolymer of the present disclosure
- the polymer electrolyte membrane includes a conventional copolymer (e.g., one that does not include one or more divalent units independently represented by formula:
- the polymer electrolyte membrane is prepared from the copolymer of the present disclosure, and the catalyst ink includes a conventional copolymer (e.g., one that does not include one or more divalent units independently represented by formula:
- a salt of at least one of cerium, manganese or ruthenium or one or more cerium oxide or zirconium oxide compounds is added to the acid form of the copolymer before membrane formation.
- the salt of cerium, manganese, or ruthenium and/or the cerium or zirconium oxide compound is mixed well with or dissolved within the copolymer to achieve substantially uniform distribution.
- the salt of cerium, manganese, or ruthenium may comprise any suitable anion, including chloride, bromide, hydroxide, nitrate, sulfonate, acetate, phosphate, and carbonate. More than one anion may be present. Other salts may be present, including salts that include other metal cations or ammonium cations. Once cation exchange occurs between the transition metal salt and the acid form of the ionomer, it may be desirable for the acid formed by combination of the liberated proton and the original salt anion to be removed. Thus, it may be useful to use anions that generate volatile or soluble acids, for example chloride or nitrate.
- Manganese cations may be in any suitable oxidation state, including Mn 2+ , Mn + , and Mn 4+ , but are most typically Mn 2+ .
- Ruthenium cations may be in any suitable oxidation state, including Ru + and Ru 4+ , but are most typically Ru + .
- Cerium cations may be in any suitable oxidation state, including Ce + and Ce 4+ . Without wishing to be bound by theory, it is believed that the cerium, manganese, or ruthenium cations persist in the polymer electrolyte because they are exchanged with H + ions from the anion groups of the polymer electrolyte and become associated with those anion groups. Furthermore, it is believed that polyvalent cerium, manganese, or ruthenium cations may form crosslinks between anion groups of the polymer electrolyte, further adding to the stability of the polymer. In some embodiments, the salt may be present in solid form.
- the cations may be present in a combination of two or more forms including solvated cation, cation associated with bound anion groups of the polymer electrolyte membrane, and cation bound in a salt precipitate.
- the amount of salt added is typically between 0.001 and 0.5 charge equivalents based on the molar amount of acid functional groups present in the polymer electrolyte, more typically between 0.005 and 0.2, more typically between 0.01 and 0.1, and more typically between 0.02 and 0.05.
- Further details for combining an anionic copolymer with cerium, manganese, or ruthenium cations can be found in U.S. Pat. Nos. 7,575,534 and 8,628,871, each to Frey et al..
- the cerium oxide compound may contain cerium in the (IV) oxidation state, the (III) oxidation state, or both and may be crystalline or amorphous.
- the cerium oxide may be, for example, Ce02 or Ce203.
- the cerium oxide may be substantially free of metallic cerium or may contain metallic cerium.
- the cerium oxide may be, for example, a thin oxidation reaction product on a metallic cerium particle.
- the cerium oxide compound may or may not contain other metal elements. Examples of mixed metal oxide compounds comprising cerium oxide include solid solutions such as zirconia-ceria and multicomponent oxide compounds such as barium cerate. Without wishing to be bound by theory, it is believed that the cerium oxide may strengthen the polymer by chelating and forming crosslinks between bound anionic groups.
- the amount of cerium oxide compound added is typically between 0.01 and 5 weight percent based on the total weight of the copolymer, more typically between 0.1 and 2 weight percent, and more typically between 0.2 and 0.3 weight percent.
- the cerium oxide compound is typically present in an amount of less than 1% by volume relative to the total volume of the polymer electrolyte membrane, more typically less than 0.8% by volume, and more typically less than 0.5% by volume.
- Cerium oxide may be in particles of any suitable size, in some embodiments, between 1 nm and 5000 nm, 200 nm to 5000 nm, or 500 nm to 1000 nm. Further details regarding polymer electrolyte membranes including cerium oxide compounds can be found in U.S. Pat. No. 8,367,267 (Frey et al.).
- the polymer electrolyte membrane in some embodiments, may have a thickness of up to 90 microns, up to 60 microns, or up to 30 microns.
- a thinner membrane may provide less resistance to the passage of ions. In fuel cell use, this results in cooler operation and greater output of usable energy. Thinner membranes must be made of materials that maintain their structural integrity in use.
- the copolymer of the present disclosure may be imbibed into a porous supporting matrix, typically in the form of a thin membrane having a thickness of up to 90 microns, up to 60 microns, or up to 30 microns. Any suitable method of imbibing the copolymer into the pores of the supporting matrix may be used, including overpressure, vacuum, wicking, and immersion.
- the copolymer is embedded in the matrix upon crosslinking.
- Any suitable supporting matrix may be used.
- the supporting matrix is electrically non- conductive.
- the supporting matrix is composed of a fluoropolymer, which is more typically perfluorinated.
- Typical matrices include porous polytetrafluoroethylene (PTFE), such as biaxially stretched PTFE webs.
- fillers e.g. fibers might be added to the polymer to reinforce the membrane.
- GDL's may be applied to either side of a CCM by any suitable means.
- Any suitable GDL may be used in the practice of the present disclosure.
- the GDL is comprised of sheet material comprising carbon fibers.
- the GDL is a carbon fiber construction selected from woven and non-woven carbon fiber constructions.
- Carbon fiber constructions which may be useful in the practice of the present disclosure may include TorayTM Carbon Paper, SpectraCarbTM Carbon Paper, AFNTM non-woven carbon cloth, and ZoltekTM Carbon Cloth.
- the GDL may be coated or impregnated with various materials, including carbon particle coatings, hydrophilizing treatments, and hydrophobizing treatments such as coating with polytetrafluoroethylene (PTFE).
- PTFE polytetrafluoroethylene
- the MEA according to the present disclosure is typically sandwiched between two rigid plates, known as distribution plates, also known as bipolar plates (BPP's) or monopolar plates.
- the distribution plate is typically electrically conductive.
- the distribution plate is typically made of a carbon composite, metal, or plated metal material.
- the distribution plate distributes reactant or product fluids to and from the MEA electrode surfaces, typically through one or more fluid-conducting channels engraved, milled, molded or stamped in the surface(s) facing the MEA(s). These channels are sometimes designated a flow field.
- the distribution plate may distribute fluids to and from two consecutive MEA's in a stack, with one face directing fuel to the anode of the first MEA while the other face directs oxidant to the cathode of the next MEA (and removes product water), hence the term "bipolar plate.”
- the distribution plate may have channels on one side only, to distribute fluids to or from an MEA on only that side, which may be termed a "monopolar plate.”
- a typical fuel cell stack comprises a number of MEA's stacked alternately with bipolar plates.
- An electrolysis cell which uses electricity to produce chemical changes or chemical energy.
- An example of an electrolysis cell is a chlor-alkali membrane cell where aqueous sodium chloride is electrolyzed by an electric current between an anode and a cathode. The electrolyte is separated into an anolyte portion and a catholyte portion by a membrane subject to harsh conditions.
- caustic sodium hydroxide collects in the catholyte portion, hydrogen gas is evolved at the cathode portion, and chlorine gas is evolved from the sodium chloride-rich anolyte portion at the anode.
- the copolymer of the present disclosure may be useful, for example, in the manufacture of catalyst ink and electrolyte membranes for use in chlor-alkali membrane cells or other electrolytic cells.
- the copolymer according to the present disclosure may also be useful has a binder for an electrode in other electrochemical cells (for example, lithium ion batteries).
- a binder for an electrode in other electrochemical cells for example, lithium ion batteries.
- powdered active ingredients can be dispersed in a solvent with the copolymer and coated onto a metal foil substrate, or current collector.
- the resulting composite electrode contains the powdered active ingredient in the polymer binder adhered to the metal substrate.
- Useful active materials for making negative electrodes include alloys of main group elements and conductive powders such as graphite.
- useful active materials for making a negative electrode include oxides (tin oxide), carbon compounds (e.g., artificial graphite, natural graphite, soil black lead, expanded graphite, and scaly graphite), silicon carbide compounds, silicon-oxide compounds, titanium sulfides, and boron carbide compounds.
- Useful active materials for making positive electrodes include lithium compounds, such as Li4/3Ti5/304, L1V3O8, L1V2O5, LiCoo.2Nio.8O2, LiNiC>2,
- the electrodes can also include electrically conductive diluents and adhesion promoters.
- Electrochemical cells including the copolymer disclosed herein as a binder can be made by placing at least one each of a positive electrode and a negative electrode in an electrolyte.
- a microporous separator can be used to prevent the contact of the negative electrode directly with the positive electrode. Once the electrodes are connected externally, lithiation and delithiation can take place at the electrodes, generating a current.
- electrolytes can be employed in a lithium-ion cell. Representative electrolytes contain one or more lithium salts and a charge-carrying medium in the form of a solid, liquid, or gel. Examples of lithium salts include LiPFe, LiBF 4 , L1CIO4, lithium bis(oxalato)borate, LiN(CF 3 S0 2 ) 2 , LiN(C 2 F 5 S0 2 )2, LiAsF 6 , LiC(CF3SC>2)3, and combinations thereof.
- solid charge carrying media examples include polymeric media such as polyethylene oxide, polytetrafluoroethylene, polyvinylidene fluoride, fluorine-containing copolymers, polyacrylonitrile, combinations thereof, and other solid media that will be familiar to those skilled in the art.
- liquid charge carrying media examples include ethylene carbonate, propylene carbonate, dimethyl carbonate, diethyl carbonate, ethyl methyl carbonate, butylene carbonate, vinylene carbonate, fluoroethylene carbonate, fluoropropylene carbonate, gamma-butyrolactone, methyl difluoroacetate, ethyl difluoroacetate, dimethoxyethane, diglyme (bis(2-methoxyethyl) ether), tetrahydrofuran, dioxolane, combinations thereof and other media that will be familiar to those skilled in the art.
- charge carrying media gels include those described in U.S. Pat. Nos. 6,387,570 (Nakamura et al.) and 6,780,544 (Noh).
- the electrolyte can include other additives (e.g., a cosolvent or a redox chemical shuttle).
- the electrochemical cells can be useful as rechargeable batteries and can be used in a variety of devices, including portable computers, tablet displays, personal digital assistants, mobile telephones, motorized devices (e.g., personal or household appliances and vehicles), instruments, illumination devices (e.g., flashlights) and heating devices.
- portable computers tablet displays, personal digital assistants, mobile telephones, motorized devices (e.g., personal or household appliances and vehicles), instruments, illumination devices (e.g., flashlights) and heating devices.
- One or more of the electrochemical cells can be combined to provide battery pack.
- the present disclosure provides a copolymer comprising:
- a is 0 or 1
- b is 2 to 8
- c is 0 to 2
- e is 1 to 8
- Z is independently a hydrogen, alkyl having up to four carbon atoms, an alkali-metal cation, or a quaternary ammonium cation; and one or more divalent units independently represented by formula:
- Rf is a linear or branched perfluoroalkyl group having from 1 to 8 carbon atoms and optionally interrupted by one or more -O- groups, z is 0, 1, or 2, each n is independently 1, 2, 3, or 4, and m is 0 or 1 ;
- the copolymer when Z is hydrogen, has an alpha transition temperature of up to 100 ° C or less than 100 ° C, wherein the copolymer has an -SO3Z equivalent weight in a range from 300 to 1400, and wherein a variation of the copolymer in which -SO3Z is replaced with - SO2F has a melt flow index of up to 80 grams per ten minutes measured at a temperature of 265 ° C and at a support weight of 5 kg.
- the present disclosure provides the copolymer of the first embodiment, wherein b is 2 or 3, c is 0 or 1, and e is 4.
- the present disclosure provides the copolymer of the first embodiment, wherein b is 2 or 3, c is 1, and e is 2 or 4.
- the present disclosure provides the copolymer of any one of the first to third embodiments, wherein when a is 0, then n is not 3.
- the present disclosure provides the copolymer of any one of the first to fourth embodiments, wherein z is 1 or 2, and n is 1, 2, or 3.
- the present disclosure provides the copolymer of any one of the first to fifth embodiments, wherein at least one n is 1.
- the present disclosure provides the copolymer of any one of the first to sixth embodiments, at least one of c is 1 or 2 or e is 3 to 8.
- the present disclosure provides the copolymer of any one of the first to seventh embodiments, wherein a is 1.
- the present disclosure provides the copolymer of any one of the first to seventh embodiments, wherein a is 0.
- the present disclosure provides the copolymer of any one of the first to ninth embodiments, wherein the copolymer further comprises at least one of divalent units derived from chlorotrifluoroethylene or divalent units derived from hexafluoropropylene.
- the present disclosure provides the copolymer of any one of the first to tenth embodiments, wherein the copolymer has a T(a) of at least 60 ° C.
- the present disclosure provides the copolymer of any one of the first to eleventh embodiments, wherein the copolymer further comprises divalent units independently represented by formula:
- Z' is a hydrogen, an alkyl group having up to four carbon atoms, an alkali-metal cation or a quaternary ammonium cation.
- the present disclosure provides the copolymer of any one of the first to twelfth embodiments, wherein the divalent units comprise at least 60 mole % of -[CF2- CF2]-, based on the total amount of divalent units in the copolymer.
- the present disclosure provides the copolymer of the fourteenth embodiment, wherein X, Y, and W are each independently fluoro, CF3, C2F5, C3F7, C4F9, hydrogen, CH 3 , C 2 H 5 , C3H7, C 4 H 9 .
- the present disclosure provides the copolymer of any one of the first to fifteenth embodiments, wherein Z is hydrogen
- the present disclosure provides the copolymer of any one of the first to fifteenth embodiment, wherein Z is sodium.
- the present disclosure provides the copolymer of any one of the first to seventeenth embodiments, wherein the copolymer has an -SO2X equivalent weight in a range from 400 to 1200.
- the present disclosure provides the copolymer of any one of the first to eighteenth embodiments, wherein the copolymer further comprises divalent units derived from at least one of ethylene, propylene, isobutylene, ethyl vinyl ether, vinyl benzoate, ethyl allyl ether, cyclohexyl allyl ether, norbornadiene, crotonic acid, an alkyl crotonate, acrylic acid, an alkyl acrylate, methacrylic acid, an alkyl methacrylate, or hydroxybutyl vinyl ether.
- the present disclosure provides the copolymer of any one of the first to nineteenth embodiments, wherein the copolymer has up to 100 -COOM and -COF end groups per 10 6 carbon atoms, wherein M is independently an alkyl group, a hydrogen atom, a metallic cation, or a quaternary ammonium cation.
- the present disclosure provides the copolymer of any one of the first to twentieth embodiments, wherein the copolymer comprises less than 25 ppm metal ions.
- the present disclosure provides the copolymer of any one of the first to twenty-first embodiments, wherein the copolymer comprises -SO2X end groups.
- the present disclosure provides the copolymer of any one of the first to twenty-second embodiments, wherein the variation of the copolymer in which -SO3Z is replaced with-S02F has a melt flow index of up to 40 grams per ten minutes measured at a temperature of 265 ° C and at a support weight of 5 kg.
- the present disclosure provides the copolymer of any one of the first to twenty-third embodiments, wherein the variation of the copolymer in which -SO3Z is replaced with -SO2F has a glass transition temperature of up to 20 ° C.
- the present disclosure provides the copolymer of any one of the first to twenty-fourth embodiments, wherein the divalent units represented by formula
- the present disclosure provides the copolymer of any one of the first to twenty-fifth embodiments, wherein the divalent units represented by formula are present at up to 30 or up to 25 mole percent, or in a range from 10 to 30 or 15 to 25 mole percent, based on the total moles of divalent units in the copolymer.
- the present disclosure provides a polymer electrolyte membrane comprising the copolymer of any one of the first to twenty-sixth embodiments.
- the present disclosure provides the polymer electrolyte membrane of the twenty-seventh embodiment, wherein the polymer electrolyte membrane further comprises at least one of cerium cations, manganese cations, ruthenium cations, or a cerium oxide.
- the present disclosure provides the polymer electrolyte membrane of the twenty-eighth embodiment, wherein the at least one of cerium cations, manganese cations, or ruthenium cations are present in a range from 0.2 to 20 percent relative to the amount of sulfonate groups in the copolymer.
- the present disclosure provides a catalyst ink comprising the copolymer of any one of the first to twenty-sixth embodiments.
- the present disclosure provides a membrane electrode assembly comprising at least one of the polymer electrolyte membrane of any one of the twenty- seventh to twenty-ninth embodiments or the catalyst ink of the thirtieth embodiment.
- the present disclosure provides a binder for an electrode comprising the copolymer of any one of the first to twenty-sixth embodiments.
- the present disclosure provides an electrochemical cell comprising the binder of the thirty -second embodiment.
- the present disclosure provides a copolymer comprising: divalent units represented by formula -[CF2-CF2]-;
- a is 0 or 1
- b is 2 to 8
- c is 0 to 2
- e is 1 to 8
- Rf is a linear or branched perfluoroalkyl group having from 1 to 8 carbon atoms and optionally interrupted by one or more -O- groups, z is 0, 1, or 2, each n is independently 1, 2, 3, or 4, and m is 0 or 1 ;
- the copolymer has an -SO2F equivalent weight in a range from 300 to 1400 and a melt flow index of up to 80 grams per ten minutes measured at a temperature of 265 ° C and at a support weight of 5 kg, and wherein when the copolymer is hydrolyzed such that the -SO2F is replaced by -SO3H, the copolymer has an alpha transition temperature of up to 100 ° C.
- the present disclosure provides the copolymer of the thirty- fourth embodiment, wherein b is 2 or 3, c is 0 or 1, and e is 4.
- the present disclosure provides the copolymer of the thirty- fourth embodiment, wherein b is 2 or 3, c is 1, and e is 2 or 4.
- the present disclosure provides the copolymer of any one of the thirty-fourth to thirty-sixth embodiments, wherein when a is 0, then n is not 3.
- the present disclosure provides the copolymer of any one of the thirty-fourth to thirty-seventh embodiments, wherein z is 1 or 2, and n is 1, 2, or 3.
- the present disclosure provides the copolymer of any one of the thirty-fourth to thirty-eighth embodiments, wherein at least one n is i .
- the present disclosure provides the copolymer of any one of the thirty-fourth to thirty-ninth embodiments, at least one of c is 1 or 2 or e is 3 to 8.
- the present disclosure provides the copolymer of any one of the thirty-fourth to fortieth embodiments, wherein the copolymer further comprises at least one of divalent units derived from chlorotrifluoroethylene or divalent units derived from
- the present disclosure provides the copolymer of any one of the thirty-fourth to forty-first embodiments, wherein the copolymer has a T(a) of at least 60 ° C.
- the present disclosure provides the copolymer of any one of the thirty-fourth to forty-second embodiments, wherein the copolymer further comprises divalent units independently represented by formula:
- Z' is a hydrogen, an alkyl group having up to four carbon atoms, an alkali-metal cation or a quaternary ammonium cation.
- the present disclosure provides the copolymer of any one of the thirty-fourth to forty-third embodiments, wherein the divalent units comprise at least 60 mole % of
- n, o are independently 0 or 1, or wherein X, Y, and W are each independently fluoro, CF3, C2F5, C3F7, C4F9, hydrogen, Ct1 ⁇ 4, C2H5, C3H7, C4H9.
- the present disclosure provides the copolymer of any one of the thirty-fourth to forty-fifth embodiments, wherein the copolymer has an -SO 2 X equivalent weight in a range from 400 to 1200.
- the present disclosure provides the copolymer of any one of the thirty-fourth to forty-sixth embodiments, wherein the copolymer further comprises divalent units derived from at least one of ethylene, propylene, isobutylene, ethyl vinyl ether, vinyl benzoate, ethyl allyl ether, cyclohexyl allyl ether, norbomadiene, crotonic acid, an alkyl crotonate, acrylic acid, an alkyl acrylate, methacrylic acid, an alkyl methacrylate, or hydroxybutyl vinyl ether.
- the present disclosure provides the copolymer of any one of the thirty-fourth to forty-seventh embodiments, wherein the copolymer has up to 100 -COOM and -COF end groups per 10 6 carbon atoms, wherein M is independently an alkyl group, a hydrogen atom, a metallic cation, or a quaternary ammonium cation, and/or
- copolymer comprises less than 25 ppm metal ions, and/or
- copolymer comprises -SO2X end groups.
- the present disclosure provides the copolymer of any one of the thirty-fourth to forty-eighth embodiments, wherein the copolymer has a melt flow index of up to 40 grams per ten minutes measured at a temperature of 265 ° C and at a support weight of 5 kg.
- the present disclosure provides the copolymer of any one of the thirty-fourth to forty-ninth embodiments, wherein the copolymer has a glass transition temperature of up to 20 ° C.
- the present disclosure provides the copolymer of any one of the thirty-fourth to fiftieth embodiments, wherein the divalent units represented by formula
- Solid content was determined gravimetrically by placing samples of the dispersions on a heated balance and recording the mass before and after evaporation of solvent. The solid content was the ratio of the initial mass of the sample and the mass of the sample when the mass did not decrease further with continued heating.
- the EW of a copolymer of TFE, a sulfonyl fluoride monomer (M2), and a vinyl ether or allyl ether monomer (M3) can be calculated by the formula:
- a Fourier transform infrared spectroscopy (FT-IR) measurement can be used to determine the number of carboxyl endgroups per 10 6 C-atoms in the copolymer.
- the measurement is performed by FT-IR in a transmission technique.
- the measured sample has a film thickness of 100 ⁇ .
- the wave numbers of the COOH peaks of interest are 1776 cm “1 and 1807 cm “1 .
- the wave number of the C(0)F peak is 1885 cm “1 .
- (C(O)F will convert to a carboxyl group).
- To quantify the amount of carboxyl (C(O)F) endgroups of the polymer two IR spectra are taken. One from the carboxyl containing sample and one from a reference sample (without carboxyl groups).
- the number of endgroups per 10 6 carbon atoms can be calculated via equation 1, 2 and 3
- the particle size determination was conducted by dynamic light scattering according to ISO 13321 (1996).
- a Zeta Sizer Nano ZS available from Malvern Instruments Ltd, Malvern, Worcestershire, UK, equipped with a 50 mW laser operating at 532 nm was used for the analysis.
- 12 mm square glass cuvettes with round aperture and cap (PCS 8501, available from Malvern Instruments Ltd) were used to mount a sample volume of 1 mL. Since light scattering of surfactants is extremely sensitive to the presence of larger particles, e.g. dust particles, the presence of contaminants was minimized by thoroughly cleaning the cuvettes before the measurements.
- the cuvettes were washed with freshly-distilled acetone for 8 h in a cuvette washing device. Dust discipline was also applied to the samples by centrifuging the surfactant solutions in a laboratory centrifuge at 14,500 G (142,196 N/kg) for 10 min prior to the
- the measuring device was operated at 25 °C in 173° backscattering mode.
- Low correlation times of t ⁇ l "6 sec were enabled by the research tool (the research tool is a software upgrade of the standard instrument provided by the supplier).
- the research tool is a software upgrade of the standard instrument provided by the supplier.
- melt flow index reported in g/10 min, was measured with a Goettfert MPD
- MI-Robo, MI4 melt indexer (Buchen, Germany) following a similar procedure to that described in DIN EN ISO 1133-1 at a support weight of 5.0 kg and a temperature of 265 °C.
- the MFI was obtained with a standardized extrusion die of 2.1 mm in diameter and a length of 8.0 mm. ⁇ ( ⁇ ) Measurement
- a TA Instruments AR2000 EX rheometer was used to measure the T(a) of the polymer samples. Samples were heated on a temperature ramp from -100 °C to about 125 °C at 2 °C per minute. Measurements were made at a frequency of one hertz.
- Tg glass transition temperature
- the oxygen permeability as a function of temperature for each membrane was determined using the time lag method.
- the membranes with an active area of 1 cm 2 were placed in a permeability cell. Both chambers of the cell were subsequently evacuated for 6 hours. Time zero for the test coincided with the pressurization of upper chamber to 760 cm Hg with the challenging gas (oxygen).
- the variation of the pressure as a function of time in the evacuated lower chamber was measured using a pressure sensor (Baratron®, MKS, MA, USA) with a sensitivity of 10 cm Hg.
- the oxygen permeability P in barrer (cm stp cm / sec cm 2 cm Hg) was calculated using the following expression:
- Vb is the volume of the lower chamber in cm 3
- 1 is the membrane thickness in cm
- A is the exposed surface area of the membrane in cm 2
- T is temperature in °K
- p a is the pressure of the upper chamber in cm Hg
- R is the gas constant (6236.367 cm Hg cm 3 / mol °K)
- dp b / dt is the rate of change of the pressure in the lower chamber as a function of time measured in the linear part of the pressure - time curve (cm Hg/ sec).
- TFE tetrafluoroethylene
- M4S FzC ⁇ F-O-CFzCFzCFzSOzF
- CF 2 CF-0-(CF 2 )3-OCF 3 (MV31)
- MV4S was prepared according to the method described in U.S. Pat. No. 6,624,328 (Guerra).
- MV31 was prepared according to the method described in U.S. Pat. Nos. 6,255,536 (Worm et al.)
- a 4-L polymerization kettle equipped with an impeller agitator system was charged with ammonium oxalate monohydrate (5 g) and oxalic acid dihydrate (1 g) in 3 ⁇ 40 (2000 g) and 40 g of a 30 wt. % aqueous solution of CF3-0-(CF2)3-0-CFH-CF2-COONH4, prepared as described in "Preparation of Compound 11" in U.S. Pat. No. 7,671,112.
- the kettle was degassed and subsequently charged with nitrogen several times to assure that all of oxygen was removed.
- the kettle was purged with TFE.
- the kettle was then heated to 50 °C and the agitation system was set to 320 rpm.
- a mixture of MV4S (260 g), MV31 (50 g), and 8.6 g of the 30 wt. % CF3-0-(CF2)3-0-CFH-CF2-COONH4 solution and deionized water ( 165 g) were emulsified under high shear by an agitator available under the trade designation "ULTRA -TURRAX T 50" from TKA Works, Wilmington, NC, USA operated at 24000 rpm for 2 mm.
- the MV4S and MV31 emulsion was charged into the reaction kettle.
- the kettle was further charged with TFE (127 g) to a pressure of 6 bar (600 kPa).
- the polymerization was initiated by a 0.045 % solution of KMnOi (33 g) in deionized water.
- the reaction temperature of 50 °C as well as the reaction pressure of 6 bar (600 kPa) were maintained by feeding TFE into the gas phase.
- the continuous feeding of the MV4S and MV31 emulsion (in total 1037 g: 557 g MV4S and 106 g MV31 and 21 g of the 30 % CF3-0-(CF 2 )3-0-CFH-CF 2 -COONH 4 solution in 353 g deionized water), TFE (458 g), and of a 0.045 % solution of ⁇ . in deionized water (350 g) was continued.
- the molar ratio of the continuous feed was 72 mol % TFE, 23 mol % MV4S and 5 mol % MV31.
- the average metering rate of the continuous addition of the 0.045 % KMn04 solution was 92 g/h to obtain a polymer dispersion with a solid content of 23.2 %.
- the polymerization time was 228 min.
- the latex particle diameter was 126 nm according to dynamic light scattering.
- the polymer dispersion was charged into a 100L glass vessel equipped with a lab stirrer (PENDRAULIK). While the lab stirrer of the glass vessel was rotated to 2500 rpm, a 65 wt-% nitric acid (170 g) was fed continuously in the glass vessel to precipitate the polymer. Then the mixture was rotated for 1 h under the same stirring conditions with a final solid content of 1.4% in the polymerization medium (water phase).
- PENDRAULIK lab stirrer
- the remaining aqueous polymerization medium was removed and the wet polymerization crumb was washed seven times with 4 L DI water while the stirrer was rotated to 930 rpm.
- the pH value of the seventh washing medium was nearly 4.
- the wet polymerizate was transferred in two portions in an air circulation dryer. Each portion was dried for 17 hours at 80 °C with a final water content of ⁇ 0.1 % determined by thermobalance.
- the coagulated, washed, and dried polymer had a MFI (265 °C/5 kg) of 41 g/10 min.
- the polymer had a composition of 70.3 mol % TFE, 24.4 niol-% MV4S and 5.3 mol % MV31 as determined by l9 F-NMR-spectroscopy. This corresponded to an equivalent weight EW of 740.
- the glass transition temperature (Tg) was measured using the test method described above and found to be 3 ° C.
- the dispersion was passed through an ion exchange bed consisting of a Kimble
- Chromaflex Column with the dimensions of 38 x 500mm filled with 300mL of Amberlite IR- 120(Plus) Hydrogen Form Ion Exchange Resin.
- the resin was prepared by first flushing the column with 3 L of DI water with the stop cock completely open. After 900 mL of 5% HC1 solution was passed through the column over 30 minutes followed by 600 mL of DI water over 20 minutes. Next 3 L of DI water was passed through with the stop cock fully open. The dispersion was then ion exchanged at a rate of 1200 mL per hour. Any precipitate that formed after hydrolysis was not fed into the ion exchange column. The resin was regenerated after every 400 mL of dispersion using the same process outlined above.
- the membrane was evaluated at 30 ° C using the Oxygen Permeability evaluation method described above. A value of 161 (barrer x 10 10 ) was measured. The oxygen permeability at 50 ° C and 70 ° C was found to be higher than the detection limit.
- TFE tetrafluoroethylene
- M4S FzC ⁇ F-O-CFzCFzCFzSOzF
- CF 2 CF-0-(CF 2 )3-OCF 3 (MV31)
- MV4S and MV31 were prepared as described in Example 1.
- a 4-L polymerization kettle equipped with an impeller agitator system was charged with ammonium oxalate monohydrate (5 g) and oxalic acid dihydrate (1 g) in H2O (2000 g) and 40 g of a 30 wt. % aqueous solution of CF3-0-(CF2)3-0-CFH-CF2-COONH4.
- the kettle was degassed and subsequently charged with nitrogen several times to assure that all of oxygen was removed.
- the kettle was purged with TFE.
- the kettle was then heated to 50 °C and the agitation system was set to 320 iprn.
- a mixture of MV4S (237 g), MV31 (78 g), and 9.6 g of the 30 wt. % CF 3 -0-(CF 2 )3-0-CFH-CF2-COONH4 solution and deiomzed water (147 g) were emulsified under high shear by an agitator available under the trade designation "ULTRA - TURRAX T 50" from I A Works, operated at 24000 rpm for 2 mm.
- the MV4S and MV31 emulsion was charged into the reaction kettle.
- the kettle was further charged with TFE (126 g) to a pressure of 6 bar (600 kPa).
- the polymerization was initiated by a 0.045 % solution of KMnOi (20 g) in deionized water.
- the reaction temperature of 50 °C as well as the reaction pressure of 6 bar (600 kPa) were maintained by feeding TFE into the gas phase.
- the continuous feeding of the MV4S and MV31 emulsion in total 1128 g: 567 g MV4S and 187 g MV31 and 23 g of the 30 %
- 0.045 % solution of KMnO . in deionized water 120 g was continued.
- the average metering rate of the continuous addition of the 0.045 % KMnC solution was 37 g/h to obtain a polymer dispersion with a solid content of 19.7 %.
- the polymerization time was 194 min.
- the latex particle diameter was 114 nm according to dynamic light scattering.
- the copolymer was coagulated, washed, and dried similarly to Example 1.
- the coagulated, washed, and dried polymer had a MFI (265 °C/5 kg) of 57 g/10 min.
- the calculated equivalent weight EW was 742.
- TFE tetrafluoroethylene
- MVC FzC ⁇ F-O-CFzCFzCFzSOzF
- CF 2 CF-0-(CF 2 ) 2 -CF 3 (PPVE-1)
- a 4-L polymerization kettle with an impeller agitator system was charged with 5 g ammonium oxalate monohydrate and 1 g oxalic acid dihydrate in 2000 g H2O and 40 g of a 30 wt. % aqueous solution of CF3-0-(CF2)3-0-CFH-CF2-COONH4.
- the kettle was degassed and subsequently charged with nitrogen several times to assure that all of oxygen was removed. Afterwards, the kettle was purged with TFE, The kettle was then heated to 50 °C and the agitation system was set to 320 rpm.
- % CF 3 -0-(CF 2 ) 3 -0-CFH- CF2-COONH4 solution and 51 g deionized water were emulsified under high shear by a "ULTRA - TURJ AX T 50" agitator from IKA Works operated at 24000 rpm for 2 min.
- the MV4S-emulsion was charged into the reaction kettle.
- the kettle was further charged with 114 g TFE and 40 g PPVE- 1 to 6 bar pressure (600 kPa).
- the polymerization was initiated by 16 g of a 0.09 % solution of potassium permanganate (KMnQ 4 ) in deionized water.
- the reaction temperature of 50 °C as well as the reaction pressure of 6 bar (600 kPa) was maintained by feeding TFE and PPVE-1 into the gas phase.
- 193 g TFE, 121 g PPVE-1, and 235 g of a 0.09 % solution of KM11O4 in deionized water was continued.
- the average metering rate of the continuously addition of the 0.09 % KMn04 solution was 123 g/h to obtain a polymer dispersion with a solid content of 14.1 %.
- the polymerization time was 115 min and latex particle diameter was 150 mn according to dynamic light scattering.
- the copolymer was coagulated, washed, and dried similarly to Example 1.
- the coagulated, washed, and dried polymer had a MFI (265 °C/5 kg) of 66 g/10 min.
- the polymer showed a chemical composition of 74.2 mol-% TFE, 16.1 mol-% MV4S and 9.7 mol-% PPVE-1 as determined by 19 F- NMR-spectroscopy. This corresponds to an equivalent weight of 1000.
- the glass transition temperature (Tg) was measured using the test method described above and found to be 10 ° C.
- the polymer was hydroiyzed similarly to Example 1 except 16.2 g of LiOF FfcO, 9.5 g of L12CO3 and 129 g of the polymer was charged into the reactor. The reactor was then heated to 255 °C over a period of 114 minutes. The dispersion was ion exchanged, dried, and an n-propanol based dispersion was prepared similarly to Example 1. In Example 2, 2.14 g of ionomer was combined with 4.70g of n-propanol and 2.96 g DI H2O. A clear dispersion was formed with no visible undispersed material.
- a membrane was made similarly to Example 1.
- the T(a) was measured according to the test method above and determined to be 93 ° C.
- the membrane was evaluated at 30 ° C using the Oxygen Permeability evaluation method described above.
- a value of 2.6 (barrer x 10 10 ) was measured.
- the oxygen permeability at 50 ° C and 70 ° C was found to be 5.8 and 10.1 (barrer x 1() 10 ), respectively.
- TFE tetrafluoroethylene
- MVC FzC ⁇ F-O-CFzCFzCFzSC ⁇ F
- MV4S was prepared as described above.
- a 4-L polymerization kettle equipped with an impeller agitator system was charged with ammonium oxalate monohydrate (5 g) and oxalic acid dihydrate (1 g) in FbO (2000 g) and 40 g of a 30 wt. % aqueous solution of CF 3 -0-(CF 2 )3-0-CFH-CF2-COONH4.
- the kettle was degassed and subsequently charged with nitrogen several times to assure that all of oxygen was removed.
- the kettle was purged with TFE.
- the kettle was then heated to 50 °C and the agitation system was set to 320 rpni.
- a mixture of MV4S (200 g), 15 g of the 30 wt. % CF 3 -0-(CF 2 ) 3 -0- CFH-CF2-COONH4 solution and deionized water (360 g) were emulsified under high shear by an agitator available under the trade designation "ULTRA-TURRAX T 50" from IKA Works operated at 24000 rpm for 2 nun.
- the MV4S emulsion was charged into the reaction kettle.
- the kettle was further charged with TFE (115 g) to a pressure of 6 bar (600 kPa).
- the polymerization was initiated by a 0.06 % solution of KMn(>4 (13 g) in deionized water.
- the reaction temperature of 50 °C as well as the reaction pressure of 6 bar (600 kPa) were maintained by feeding TFE into the gas phase.
- the continuous feeding of the MV4S emulsion (in total 1234 g: 630 g MV4S and 24 g of the 30 % CF 3 -0-(CF 2 )3-0-CFH-CF2-COONH4 -solution in 580 g deionized water), TFE (450 g), and of a 0.045 % solution of KMn04 in deionized water (297 g) was continued.
- the average metering rate of the continuous addition of the 0.06 % KMnCL solution was 80 g/h to obtain a polymer dispersion with a solid content of 22 %.
- the polymerization time was 232 mill.
- the latex particle diameter was 75 nni according to dynamic light scattering.
- the copolymer was coagulated, washed, and dried similarly to Example 1.
- the coagulated, washed, and dried polymer had a MFI (265 °C/5 kg) of 38 g/10 mm.
- the so-obtained polymer showed a chemical composition of 78 mol-% TFE, 22 raol-% MV4S as determined by 19 F-NMR-spectroscopy. This corresponds to an equivalent weight of 734.
- the polymer was hydrolyzed similarly to Example 1 except the reactor was charged with 4 L of DI water, 200 g of LiOH*H 2 0, 100 g of Li 2 C0 3, and 1000 g of the polymer.
- the dispersion was ion exchanged and dried similarly to Example 1.
- a dispersion was prepared similarly to
- Example 1 The dispersion was clear with no visible undispersed material, however the dispersion was very viscous.
- To prepare a membrane another dispersion consisting of 20 wt% solids dispersed in ethanol: water at a ratio 55:45 was prepared. A clear dispersion was formed with no visible undispersed material.
- the dispersion was coated similarly to Example 1 except the film was dried at 80°C for 10 minutes and then at 200 ° C for 15 minutes. The T(a) was measured according to the test method above and determined to be 104 ° C.
- a dispersion consisting of 15 wt% ionomer, 46.75% n-propanol, and 38.25% water was prepared similarly to Example 1.
- a membrane was made similarly to Example 1 except the film was dried at 90°C for 10 minutes and then at 100 ° C for 15 minutes, and then ramped to 190 ° C for 12 minutes, and then cooled to room temperature.
- the membrane was evaluated at 30 C using the Oxygen Permeability evaluation method described above. A value of 0.64 (barrer x 10 10 ) was measured.
- the oxygen permeability at 50 ' C and 70 ' C was found to be 1.4 and 2.8 (barrer x 10 10 ), respectively.
Abstract
Description
Claims
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PCT/US2018/051104 WO2019055799A1 (en) | 2017-09-14 | 2018-09-14 | Fluorinated copolymer and compositions and articles including the same |
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EP18782277.0A Ceased EP3681917A1 (en) | 2017-09-14 | 2018-09-14 | Fluoropolymer dispersion, method for making the fluoropolymer dispersion, catalyst ink and polymer electrolyte membrane |
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EP18857229.1A Withdrawn EP3681948A4 (en) | 2017-09-14 | 2018-09-14 | Fluorinated copolymer having sulfonyl pendant groups and compositions and articles including the same |
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JP (3) | JP2020534400A (en) |
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2018
- 2018-09-14 EP EP18857361.2A patent/EP3681949A4/en not_active Withdrawn
- 2018-09-14 JP JP2020515159A patent/JP2020534400A/en active Pending
- 2018-09-14 WO PCT/US2018/051096 patent/WO2019055793A1/en unknown
- 2018-09-14 CN CN201880059351.6A patent/CN111094438B/en active Active
- 2018-09-14 KR KR1020207008644A patent/KR102601806B1/en active IP Right Grant
- 2018-09-14 KR KR1020207008482A patent/KR20200052896A/en not_active Application Discontinuation
- 2018-09-14 EP EP18782277.0A patent/EP3681917A1/en not_active Ceased
- 2018-09-14 CN CN201880059876.XA patent/CN111133015B/en active Active
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- 2018-09-14 WO PCT/US2018/051094 patent/WO2019055791A1/en unknown
- 2018-09-14 US US16/646,094 patent/US20200199259A1/en not_active Abandoned
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EP3681948A1 (en) | 2020-07-22 |
US20200199259A1 (en) | 2020-06-25 |
EP3681949A4 (en) | 2021-07-14 |
CN111094439A (en) | 2020-05-01 |
JP2020534402A (en) | 2020-11-26 |
JP2020534400A (en) | 2020-11-26 |
US11492431B2 (en) | 2022-11-08 |
EP3681917A1 (en) | 2020-07-22 |
US20200277420A1 (en) | 2020-09-03 |
JP2020534398A (en) | 2020-11-26 |
KR20200052897A (en) | 2020-05-15 |
CN111094438A (en) | 2020-05-01 |
CN111094438B (en) | 2022-11-08 |
CN111133015A (en) | 2020-05-08 |
KR20200052896A (en) | 2020-05-15 |
KR20200054213A (en) | 2020-05-19 |
WO2019055791A1 (en) | 2019-03-21 |
CN111133015B (en) | 2022-09-06 |
EP3681948A4 (en) | 2021-07-14 |
CN111094439B (en) | 2022-11-08 |
KR102601806B1 (en) | 2023-11-14 |
WO2019055799A1 (en) | 2019-03-21 |
US20200303755A1 (en) | 2020-09-24 |
US11377510B2 (en) | 2022-07-05 |
WO2019055793A1 (en) | 2019-03-21 |
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